Canonical Allele Identifier: CA1261344846

Gene: SLC4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74259230G= , CM000664.2:g.74259230G=	GRCh38
NC_000002.11:g.74486357G= , CM000664.1:g.74486357G=	GRCh37
NC_000002.10:g.74339865G=	NCBI36
NG_032663.1:g.89178C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394019.7:c.867+358C= MANE Select	ENSP00000377587.2:n.867+358C=
ENST00000425249.6:c.867+358C=	ENSP00000405678.2:n.867+358C=
ENST00000346834.8:c.867+358C=	ENSP00000251768.7:n.867+358C=
ENST00000358683.8:c.675+358C=	ENSP00000351513.4:n.675+358C=
ENST00000377632.5:c.867+358C=	ENSP00000366859.1:n.867+358C=
ENST00000377634.8:c.867+358C=	ENSP00000366861.4:n.867+358C=
ENST00000394019.6:c.867+358C=	ENSP00000377587.2:n.867+358C=
ENST00000423644.5:c.867+358C=	ENSP00000395804.2:n.867+358C=
ENST00000425249.5:c.867+358C=	ENSP00000405678.1:n.867+358C=
ENST00000451608.2:c.2031+358C=	ENSP00000416453.2:n.2031+358C=
ENST00000483195.5:n.1672+358C=
NM_021196.3:c.867+358C=	NP_067019.3:n.867+358C=
NM_133478.2:c.867+358C=	NP_597812.1:n.867+358C=
NM_133478.3:c.867+358C= MANE Select	NP_597812.1:n.867+358C=
NM_001386136.1:c.519+358C=	NP_001373065.1:n.519+358C=