Canonical Allele Identifier: CA2600433989

Gene: ACADM

Linked Data

• dbSNP Id: rs2100452281
• gnomAD v3: 1-75761026-G-T
• gnomAD v4: 1-75761026-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761026G>T , CM000663.2:g.75761026G>T	GRCh38
NC_000001.10:g.76226711G>T , CM000663.1:g.76226711G>T	GRCh37
NC_000001.9:g.75999299G>T	NCBI36
NG_007045.2:g.41669G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.946-96G>T MANE Select	ENSP00000359878.5:n.946-96G>T
ENST00000473018.3:n.3070-96G>T
ENST00000532207.6:n.1957-96G>T
ENST00000541113.6:c.850-96G>T	ENSP00000442324.2:n.850-96G>T
ENST00000679509.1:n.1908-96G>T
ENST00000679530.1:c.*714-96G>T	ENSP00000506454.1:n.*714-96G>T
ENST00000679615.1:n.2961-96G>T
ENST00000679687.1:c.508-96G>T	ENSP00000506598.1:n.508-96G>T
ENST00000679704.1:c.*712-96G>T	ENSP00000505117.1:n.*712-96G>T
ENST00000679709.1:c.*909-96G>T	ENSP00000506623.1:n.*909-96G>T
ENST00000679976.1:c.*530-96G>T	ENSP00000505565.1:n.*530-96G>T
ENST00000680166.1:n.4235-96G>T
ENST00000680315.1:n.829-96G>T
ENST00000680517.1:c.*334-96G>T	ENSP00000505803.1:n.*334-96G>T
ENST00000680582.1:n.1908-96G>T
ENST00000680613.1:c.*439-96G>T	ENSP00000506114.1:n.*439-96G>T
ENST00000680662.1:c.*860-96G>T	ENSP00000505080.1:n.*860-96G>T
ENST00000680691.1:c.*609-96G>T	ENSP00000506487.1:n.*609-96G>T
ENST00000680694.1:c.*534-96G>T	ENSP00000505658.1:n.*534-96G>T
ENST00000680743.1:c.*735-96G>T	ENSP00000505073.1:n.*735-96G>T
ENST00000680749.1:c.*231-96G>T	ENSP00000505122.1:n.*231-96G>T
ENST00000680798.1:c.*421-96G>T	ENSP00000505670.1:n.*421-96G>T
ENST00000680805.1:c.805-96G>T	ENSP00000505447.1:n.805-96G>T
ENST00000680844.1:c.*730-96G>T	ENSP00000506541.1:n.*730-96G>T
ENST00000680948.1:c.*813-96G>T	ENSP00000505441.1:n.*813-96G>T
ENST00000680964.1:c.*39-96G>T	ENSP00000505961.1:n.*39-96G>T
ENST00000681037.1:c.*2430-96G>T	ENSP00000506025.1:n.*2430-96G>T
ENST00000681063.1:c.*215-96G>T	ENSP00000506616.1:n.*215-96G>T
ENST00000681209.1:c.*601-96G>T	ENSP00000505877.1:n.*601-96G>T
ENST00000681278.1:n.1648-96G>T
ENST00000681289.1:n.4941-96G>T
ENST00000681361.1:c.*613-96G>T	ENSP00000506679.1:n.*613-96G>T
ENST00000681430.1:c.*39-96G>T	ENSP00000506301.1:n.*39-96G>T
ENST00000681446.1:c.*650-96G>T	ENSP00000506244.1:n.*650-96G>T
ENST00000681450.1:c.*617-96G>T	ENSP00000505660.1:n.*617-96G>T
ENST00000681548.1:c.*532-96G>T	ENSP00000505275.1:n.*532-96G>T
ENST00000681616.1:c.*605-96G>T	ENSP00000505111.1:n.*605-96G>T
ENST00000681621.1:c.*530-96G>T	ENSP00000505770.1:n.*530-96G>T
ENST00000681680.1:n.3041-96G>T
ENST00000681720.1:c.*401-96G>T	ENSP00000505438.1:n.*401-96G>T
ENST00000681730.1:n.1168-96G>T
ENST00000681790.1:c.688-96G>T	ENSP00000505130.1:n.688-96G>T
ENST00000681837.1:n.1562-96G>T
ENST00000681913.1:n.3192-96G>T
ENST00000681916.1:c.*714-96G>T	ENSP00000506477.1:n.*714-96G>T
ENST00000681930.1:n.3070-96G>T
ENST00000370834.9:c.1045-96G>T	ENSP00000359871.5:n.1045-96G>T
ENST00000370841.8:c.946-96G>T	ENSP00000359878.4:n.946-96G>T
ENST00000420607.6:c.958-96G>T	ENSP00000409612.2:n.958-96G>T
ENST00000481374.1:n.219-96G>T
ENST00000525808.5:c.*532-96G>T	ENSP00000434823.1:n.*532-96G>T
ENST00000526129.5:c.*730-96G>T	ENSP00000434092.1:n.*730-96G>T
ENST00000526196.5:c.*714-96G>T	ENSP00000431953.1:n.*714-96G>T
ENST00000528016.1:c.160-8151G>T	ENSP00000434284.1:n.160-8151G>T
ENST00000529059.5:n.855-96G>T
ENST00000532207.5:n.676-96G>T
ENST00000534334.5:c.*687-96G>T	ENSP00000435584.1:n.*687-96G>T
ENST00000541113.5:c.838-96G>T	ENSP00000442324.1:n.838-96G>T
NM_000016.5:c.946-96G>T	NP_000007.1:n.946-96G>T
NM_001127328.2:c.958-96G>T	NP_001120800.1:n.958-96G>T
NM_001286042.1:c.838-96G>T	NP_001272971.1:n.838-96G>T
NM_001286043.1:c.1045-96G>T	NP_001272972.1:n.1045-96G>T
NM_001286044.1:c.379-96G>T	NP_001272973.1:n.379-96G>T
NM_000016.6:c.946-96G>T MANE Select	NP_000007.1:n.946-96G>T
NM_001127328.3:c.958-96G>T	NP_001120800.1:n.958-96G>T
NM_001286042.2:c.838-96G>T	NP_001272971.1:n.838-96G>T
NM_001286043.2:c.1045-96G>T	NP_001272972.1:n.1045-96G>T
NM_001286044.2:c.379-96G>T	NP_001272973.1:n.379-96G>T