Canonical Allele Identifier: CA399782733

Gene: SLC4A1

Linked Data

• MyVariant Identifiers: chr17:g.42331922A>C (hg19) ; chr17:g.44254554A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254554A>C , CM000679.2:g.44254554A>C	GRCh38
NC_000017.10:g.42331922A>C , CM000679.1:g.42331922A>C	GRCh37
NC_000017.9:g.39687448A>C	NCBI36
NG_007498.1:g.18581T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.1999T>G MANE Select	ENSP00000262418.6:p.Ser667Ala
ENST00000262418.10:c.1999T>G	ENSP00000262418.6:p.Ser667Ala
ENST00000399246.3:c.901T>G	ENSP00000382190.3:p.Ser301Ala
NM_000342.3:c.1999T>G	NP_000333.1:p.Ser667Ala
XM_005257593.3:c.1804T>G	XP_005257650.1:p.Ser602Ala
XM_011525129.1:c.1909T>G	XP_011523431.1:p.Ser637Ala
XM_011525130.1:c.1999T>G	XP_011523432.1:p.Ser667Ala
XM_011525131.1:c.1999T>G	XP_011523433.1:p.Ser667Ala
XM_005257593.5:c.1804T>G	XP_005257650.1:p.Ser602Ala
XM_011525129.2:c.1909T>G	XP_011523431.1:p.Ser637Ala
NM_000342.4:c.1999T>G MANE Select	NP_000333.1:p.Ser667Ala