Canonical Allele Identifier: CA2646249157
Gene: ACADM HGNC NCBI

Linked Data

gnomAD v4: 1-75762622-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75762622T>C , CM000663.2:g.75762622T>C GRCh38
NC_000001.10:g.76228307T>C , CM000663.1:g.76228307T>C GRCh37
NC_000001.9:g.76000895T>C NCBI36
NG_007045.2:g.43265T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1195-70T>C MANE Select ENSP00000359878.5:n.1195-70T>C
ENST00000473018.3:n.3319-70T>C
ENST00000532207.6:n.3457T>C
ENST00000541113.6:c.1099-70T>C ENSP00000442324.2:n.1099-70T>C
ENST00000679509.1:n.3408T>C
ENST00000679530.1:c.*963-70T>C ENSP00000506454.1:n.*963-70T>C
ENST00000679615.1:n.4461T>C
ENST00000679687.1:c.757-70T>C ENSP00000506598.1:n.757-70T>C
ENST00000679704.1:c.*961-70T>C ENSP00000505117.1:n.*961-70T>C
ENST00000679709.1:c.*1158-70T>C ENSP00000506623.1:n.*1158-70T>C
ENST00000679976.1:c.*779-70T>C ENSP00000505565.1:n.*779-70T>C
ENST00000680166.1:n.4484-70T>C
ENST00000680315.1:n.2329T>C
ENST00000680517.1:c.*1834T>C ENSP00000505803.1:n.*1834T>C
ENST00000680582.1:n.2157-70T>C
ENST00000680613.1:c.*688-70T>C ENSP00000506114.1:n.*688-70T>C
ENST00000680662.1:c.*1109-70T>C ENSP00000505080.1:n.*1109-70T>C
ENST00000680691.1:c.*858-70T>C ENSP00000506487.1:n.*858-70T>C
ENST00000680694.1:c.*783-70T>C ENSP00000505658.1:n.*783-70T>C
ENST00000680743.1:c.*984-70T>C ENSP00000505073.1:n.*984-70T>C
ENST00000680749.1:c.*480-70T>C ENSP00000505122.1:n.*480-70T>C
ENST00000680798.1:c.*1921T>C ENSP00000505670.1:n.*1921T>C
ENST00000680805.1:c.1054-70T>C ENSP00000505447.1:n.1054-70T>C
ENST00000680844.1:c.*2230T>C ENSP00000506541.1:n.*2230T>C
ENST00000680948.1:c.*1062-70T>C ENSP00000505441.1:n.*1062-70T>C
ENST00000680964.1:c.*1539T>C ENSP00000505961.1:n.*1539T>C
ENST00000681037.1:c.*2679-70T>C ENSP00000506025.1:n.*2679-70T>C
ENST00000681063.1:c.*464-70T>C ENSP00000506616.1:n.*464-70T>C
ENST00000681209.1:c.*850-70T>C ENSP00000505877.1:n.*850-70T>C
ENST00000681278.1:n.1897-70T>C
ENST00000681289.1:n.5190-70T>C
ENST00000681361.1:c.*2113T>C ENSP00000506679.1:n.*2113T>C
ENST00000681430.1:c.*288-70T>C ENSP00000506301.1:n.*288-70T>C
ENST00000681446.1:c.*2150T>C ENSP00000506244.1:n.*2150T>C
ENST00000681450.1:c.*866-70T>C ENSP00000505660.1:n.*866-70T>C
ENST00000681548.1:c.*2032T>C ENSP00000505275.1:n.*2032T>C
ENST00000681616.1:c.*2105T>C ENSP00000505111.1:n.*2105T>C
ENST00000681621.1:c.*2030T>C ENSP00000505770.1:n.*2030T>C
ENST00000681680.1:n.4541T>C
ENST00000681720.1:c.*650-70T>C ENSP00000505438.1:n.*650-70T>C
ENST00000681730.1:n.1417-70T>C
ENST00000681790.1:c.937-70T>C ENSP00000505130.1:n.937-70T>C
ENST00000681837.1:n.3062T>C
ENST00000681913.1:n.3441-70T>C
ENST00000681916.1:c.*963-70T>C ENSP00000506477.1:n.*963-70T>C
ENST00000681930.1:n.4570T>C
ENST00000370834.9:c.1294-70T>C ENSP00000359871.5:n.1294-70T>C
ENST00000370841.8:c.1195-70T>C ENSP00000359878.4:n.1195-70T>C
ENST00000420607.6:c.1207-70T>C ENSP00000409612.2:n.1207-70T>C
ENST00000481374.1:n.468-671T>C
ENST00000525808.5:c.*781-70T>C ENSP00000434823.1:n.*781-70T>C
ENST00000526196.5:c.*963-70T>C ENSP00000431953.1:n.*963-70T>C
ENST00000528016.1:c.160-6555T>C ENSP00000434284.1:n.160-6555T>C
ENST00000529059.5:n.1104-70T>C
ENST00000541113.5:c.1087-70T>C ENSP00000442324.1:n.1087-70T>C
NM_000016.5:c.1195-70T>C NP_000007.1:n.1195-70T>C
NM_001127328.2:c.1207-70T>C NP_001120800.1:n.1207-70T>C
NM_001286042.1:c.1087-70T>C NP_001272971.1:n.1087-70T>C
NM_001286043.1:c.1294-70T>C NP_001272972.1:n.1294-70T>C
NM_001286044.1:c.628-70T>C NP_001272973.1:n.628-70T>C
NM_000016.6:c.1195-70T>C MANE Select NP_000007.1:n.1195-70T>C
NM_001127328.3:c.1207-70T>C NP_001120800.1:n.1207-70T>C
NM_001286042.2:c.1087-70T>C NP_001272971.1:n.1087-70T>C
NM_001286043.2:c.1294-70T>C NP_001272972.1:n.1294-70T>C
NM_001286044.2:c.628-70T>C NP_001272973.1:n.628-70T>C