Canonical Allele Identifier: CA1261328336

Gene: SLC4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74222175G= , CM000664.2:g.74222175G=	GRCh38
NC_000002.11:g.74449302G= , CM000664.1:g.74449302G=	GRCh37
NC_000002.10:g.74302810G=	NCBI36
NG_032663.1:g.126233C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394019.7:c.3332-674C= MANE Select	ENSP00000377587.2:n.3332-674C=
ENST00000425249.6:c.*58-674C=	ENSP00000405678.2:n.*58-674C=
ENST00000637036.1:c.400-674C=	ENSP00000490698.1:n.400-674C=
ENST00000346834.8:c.3380-674C=	ENSP00000251768.7:n.3380-674C=
ENST00000358683.8:c.3026-674C=	ENSP00000351513.4:n.3026-674C=
ENST00000377632.5:c.3089-674C=	ENSP00000366859.1:n.3089-674C=
ENST00000377634.8:c.3380-674C=	ENSP00000366861.4:n.3380-674C=
ENST00000394019.6:c.3332-674C=	ENSP00000377587.2:n.3332-674C=
ENST00000423644.5:c.3332-674C=	ENSP00000395804.2:n.3332-674C=
ENST00000451608.2:c.4560-674C=	ENSP00000416453.2:n.4560-674C=
ENST00000480696.1:n.180-674C=
ENST00000483195.5:n.3958-674C=
NM_021196.3:c.3380-674C=	NP_067019.3:n.3380-674C=
NM_133478.2:c.3332-674C=	NP_597812.1:n.3332-674C=
NM_133478.3:c.3332-674C= MANE Select	NP_597812.1:n.3332-674C=
NM_001386136.1:c.2984-674C=	NP_001373065.1:n.2984-674C=