Canonical Allele Identifier: CA1139994556

Gene: VCAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100731231G= , CM000663.2:g.100731231G=	GRCh38
NC_000001.10:g.101196787G= , CM000663.1:g.101196787G=	GRCh37
NC_000001.9:g.100969375G=	NCBI36
NG_023034.2:g.16491G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001078.4:c.1238G= MANE Select	NP_001069.1:p.Gly413=
ENST00000294728.7:c.1238G= MANE Select	ENSP00000294728.2:p.Gly413=
NM_001078.3:c.1238G=	NP_001069.1:p.Gly413=
NM_001199834.1:c.1052G=	NP_001186763.1:p.Gly351=
NM_001199834.2:c.1052G=	NP_001186763.1:p.Gly351=
NM_080682.2:c.962G=	NP_542413.1:p.Gly321=
NM_080682.3:c.962G=	NP_542413.1:p.Gly321=
ENST00000294728.6:c.1238G=	ENSP00000294728.2:p.Gly413=
ENST00000347652.6:c.962G=	ENSP00000304611.2:p.Gly321=
ENST00000370115.1:c.929-1187G=	ENSP00000359133.1:n.929-1187G=
ENST00000370119.8:c.1052G=	ENSP00000359137.3:p.Gly351=
ENST00000650339.1:c.*787G=	ENSP00000497582.1:n.*787G=