Canonical Allele Identifier: CA1792016654

Gene: SLCO5A1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.69768748G= , CM000670.2:g.69768748G=	GRCh38
NC_000008.10:g.70680983G= , CM000670.1:g.70680983G=	GRCh37
NC_000008.9:g.70843537G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_030958.3:c.908-6873C= MANE Select	NP_112220.2:n.908-6873C=
ENST00000260126.9:c.908-6873C= MANE Select	ENSP00000260126.3:n.908-6873C=
NM_001146008.1:c.908-6873C=	NP_001139480.1:n.908-6873C=
NM_001146008.2:c.908-6873C=	NP_001139480.1:n.908-6873C=
NM_001146009.1:c.908-6873C=	NP_001139481.1:n.908-6873C=
NM_030958.2:c.908-6873C=	NP_112220.2:n.908-6873C=
ENST00000260126.8:c.908-6873C=	ENSP00000260126.3:n.908-6873C=
ENST00000524945.5:c.908-6873C=	ENSP00000434422.1:n.908-6873C=
ENST00000526750.1:c.907+63019C=	ENSP00000432676.1:n.907+63019C=
ENST00000528658.1:n.1517-6873C=
ENST00000530307.1:c.908-6873C=	ENSP00000431611.1:n.908-6873C=
ENST00000532388.5:n.1573-6873C=
XM_005251313.2:c.908-6873C=	XP_005251370.1:n.908-6873C=
XM_017013883.1:c.908-6873C=	XP_016869372.1:n.908-6873C=
XM_017013884.1:c.908-6873C=	XP_016869373.1:n.908-6873C=
XM_017013885.1:c.-6+4173C=	XP_016869374.1:n.-6+4173C=
XM_017013886.1:c.908-6873C=	XP_016869375.1:n.908-6873C=
XR_428341.2:n.1615-6873C=
XR_928814.1:n.1615-6873C=