Canonical Allele Identifier: CA2211968489

Gene: ACSM5

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20438127T= , CM000678.2:g.20438127T=	GRCh38
NC_000016.9:g.20449449T= , CM000678.1:g.20449449T=	GRCh37
NC_000016.8:g.20356950T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000331849.8:c.1536+760T= MANE Select	ENSP00000327916.4:n.1536+760T=
ENST00000577024.1:n.449+760T=
NM_017888.2:c.1536+760T=	NP_060358.2:n.1536+760T=
XM_006721055.2:c.1536+760T=	XP_006721118.1:n.1536+760T=
XM_006721056.2:c.1536+760T=	XP_006721119.1:n.1536+760T=
NM_001324371.1:c.1536+760T=	NP_001311300.1:n.1536+760T=
NM_001324372.1:c.1536+760T=	NP_001311301.1:n.1536+760T=
NM_017888.3:c.1536+760T= MANE Select	NP_060358.2:n.1536+760T=
NM_001324371.2:c.1536+760T=	NP_001311300.1:n.1536+760T=
NM_001324372.2:c.1536+760T=	NP_001311301.1:n.1536+760T=