Canonical Allele Identifier: CA418539471

Gene: ACADM

Linked Data

• ClinVar Variation Id: 1650534
• ClinVar RCV Id: RCV002149061
• dbSNP Id: rs1647211756
• MyVariant Identifiers: chr1:g.76200484T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75734799T>C , CM000663.2:g.75734799T>C	GRCh38
NC_000001.10:g.76200484T>C , CM000663.1:g.76200484T>C	GRCh37
NC_000001.9:g.75973072T>C	NCBI36
NG_007045.2:g.15442T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.396T>C MANE Select	ENSP00000359878.5:p.Pro132=
ENST00000473018.3:n.2520T>C
ENST00000525881.6:n.1358T>C
ENST00000541113.6:c.396T>C	ENSP00000442324.2:p.Pro132=
ENST00000679509.1:n.1358T>C
ENST00000679530.1:c.*164T>C	ENSP00000506454.1:n.*164T>C
ENST00000679615.1:n.2520T>C
ENST00000679687.1:c.31-5181T>C	ENSP00000506598.1:n.31-5181T>C
ENST00000679704.1:c.*162T>C	ENSP00000505117.1:n.*162T>C
ENST00000679709.1:c.*359T>C	ENSP00000506623.1:n.*359T>C
ENST00000679804.1:n.207+1877T>C
ENST00000679976.1:c.295T>C	ENSP00000505565.1:p.Tyr99His
ENST00000680166.1:n.3685T>C
ENST00000680517.1:c.286+1877T>C	ENSP00000505803.1:n.286+1877T>C
ENST00000680582.1:n.1358T>C
ENST00000680613.1:c.396T>C	ENSP00000506114.1:p.Pro132=
ENST00000680662.1:c.*310T>C	ENSP00000505080.1:n.*310T>C
ENST00000680691.1:c.*59T>C	ENSP00000506487.1:n.*59T>C
ENST00000680694.1:c.295T>C	ENSP00000505658.1:p.Tyr99His
ENST00000680743.1:c.*63T>C	ENSP00000505073.1:n.*63T>C
ENST00000680749.1:c.396T>C	ENSP00000505122.1:p.Pro132=
ENST00000680798.1:c.295T>C	ENSP00000505670.1:p.Tyr99His
ENST00000680805.1:c.396T>C	ENSP00000505447.1:p.Pro132=
ENST00000680844.1:c.*180T>C	ENSP00000506541.1:n.*180T>C
ENST00000680948.1:c.*263T>C	ENSP00000505441.1:n.*263T>C
ENST00000680964.1:c.396T>C	ENSP00000505961.1:p.Pro132=
ENST00000681037.1:c.396T>C	ENSP00000506025.1:p.Pro132=
ENST00000681063.1:c.396T>C	ENSP00000506616.1:p.Pro132=
ENST00000681209.1:c.*160T>C	ENSP00000505877.1:n.*160T>C
ENST00000681278.1:n.753T>C
ENST00000681289.1:n.753T>C
ENST00000681361.1:c.*63T>C	ENSP00000506679.1:n.*63T>C
ENST00000681430.1:c.396T>C	ENSP00000506301.1:p.Pro132=
ENST00000681446.1:c.295T>C	ENSP00000506244.1:p.Tyr99His
ENST00000681450.1:c.*63T>C	ENSP00000505660.1:n.*63T>C
ENST00000681548.1:c.*54+1877T>C	ENSP00000505275.1:n.*54+1877T>C
ENST00000681616.1:c.*164T>C	ENSP00000505111.1:n.*164T>C
ENST00000681621.1:c.295T>C	ENSP00000505770.1:p.Tyr99His
ENST00000681680.1:n.2520T>C
ENST00000681720.1:c.*54+1877T>C	ENSP00000505438.1:n.*54+1877T>C
ENST00000681730.1:n.618T>C
ENST00000681790.1:c.138T>C	ENSP00000505130.1:p.Pro46=
ENST00000681837.1:n.1012T>C
ENST00000681913.1:n.2520T>C
ENST00000681916.1:c.*164T>C	ENSP00000506477.1:n.*164T>C
ENST00000681930.1:n.2520T>C
ENST00000370834.9:c.495T>C	ENSP00000359871.5:p.Pro165=
ENST00000370841.8:c.396T>C	ENSP00000359878.4:p.Pro132=
ENST00000420607.6:c.408T>C	ENSP00000409612.2:p.Pro136=
ENST00000525808.5:c.*54+1877T>C	ENSP00000434823.1:n.*54+1877T>C
ENST00000526129.5:c.*180T>C	ENSP00000434092.1:n.*180T>C
ENST00000526196.5:c.*164T>C	ENSP00000431953.1:n.*164T>C
ENST00000526930.1:n.169T>C
ENST00000529059.5:n.305T>C
ENST00000530953.6:c.119-5181T>C	ENSP00000431372.1:n.119-5181T>C
ENST00000532509.5:c.*160T>C	ENSP00000432522.1:n.*160T>C
ENST00000534334.5:c.295T>C	ENSP00000435584.1:p.Tyr99His
ENST00000541113.5:c.288T>C	ENSP00000442324.1:p.Pro96=
NM_000016.5:c.396T>C	NP_000007.1:p.Pro132=
NM_001127328.2:c.408T>C	NP_001120800.1:p.Pro136=
NM_001286042.1:c.288T>C	NP_001272971.1:p.Pro96=
NM_001286043.1:c.495T>C	NP_001272972.1:p.Pro165=
NM_001286044.1:c.-100+1877T>C	NP_001272973.1:n.-100+1877T>C
NM_000016.6:c.396T>C MANE Select	NP_000007.1:p.Pro132=
NM_001127328.3:c.408T>C	NP_001120800.1:p.Pro136=
NM_001286042.2:c.288T>C	NP_001272971.1:p.Pro96=
NM_001286043.2:c.495T>C	NP_001272972.1:p.Pro165=
NM_001286044.2:c.-100+1877T>C	NP_001272973.1:n.-100+1877T>C