Canonical Allele Identifier: CA1176710558

Gene: ACADM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75724697G= , CM000663.2:g.75724697G=	GRCh38
NC_000001.10:g.76190382G= , CM000663.1:g.76190382G=	GRCh37
NC_000001.9:g.75962970G=	NCBI36
NG_007045.2:g.5340G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000473018.3:n.267G=
ENST00000525881.6:n.267G=
ENST00000541113.6:c.-91G=	ENSP00000442324.2:n.-91G=
ENST00000679509.1:n.267G=
ENST00000679530.1:c.-91G=	ENSP00000506454.1:n.-91G=
ENST00000679615.1:n.267G=
ENST00000679976.1:c.-91G=	ENSP00000505565.1:n.-91G=
ENST00000680517.1:c.-91G=	ENSP00000505803.1:n.-91G=
ENST00000680582.1:n.267G=
ENST00000680613.1:c.-91G=	ENSP00000506114.1:n.-91G=
ENST00000680691.1:c.-91G=	ENSP00000506487.1:n.-91G=
ENST00000680694.1:c.-91G=	ENSP00000505658.1:n.-91G=
ENST00000680749.1:c.-91G=	ENSP00000505122.1:n.-91G=
ENST00000680798.1:c.-91G=	ENSP00000505670.1:n.-91G=
ENST00000680805.1:c.-91G=	ENSP00000505447.1:n.-91G=
ENST00000680964.1:c.-91G=	ENSP00000505961.1:n.-91G=
ENST00000681037.1:c.-91G=	ENSP00000506025.1:n.-91G=
ENST00000681063.1:c.-91G=	ENSP00000506616.1:n.-91G=
ENST00000681209.1:c.-91G=	ENSP00000505877.1:n.-91G=
ENST00000681278.1:n.267G=
ENST00000681289.1:n.267G=
ENST00000681361.1:c.-91G=	ENSP00000506679.1:n.-91G=
ENST00000681430.1:c.-91G=	ENSP00000506301.1:n.-91G=
ENST00000681446.1:c.-91G=	ENSP00000506244.1:n.-91G=
ENST00000681621.1:c.-91G=	ENSP00000505770.1:n.-91G=
ENST00000681680.1:n.267G=
ENST00000681790.1:c.-370G=	ENSP00000505130.1:n.-370G=
ENST00000681837.1:n.9G=
ENST00000681913.1:n.267G=
ENST00000681930.1:n.267G=
ENST00000370841.8:c.-91G=	ENSP00000359878.4:n.-91G=
ENST00000525881.5:n.7G=
ENST00000541113.5:c.-111G=	ENSP00000442324.1:n.-111G=
NM_000016.5:c.-91G=	NP_000007.1:n.-91G=
NM_001127328.2:c.-91G=	NP_001120800.1:n.-91G=
NM_001286042.1:c.-111G=	NP_001272971.1:n.-111G=
NM_001286043.1:c.-91G=	NP_001272972.1:n.-91G=
NM_001286044.1:c.-388G=	NP_001272973.1:n.-388G=