Canonical Allele Identifier: CA500618562

Gene: SLC4A1

Linked Data

• MyVariant Identifiers: chr17:g.42328587G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44251219G>C , CM000679.2:g.44251219G>C	GRCh38
NC_000017.10:g.42328587G>C , CM000679.1:g.42328587G>C	GRCh37
NC_000017.9:g.39684113G>C	NCBI36
NG_007498.1:g.21916C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.2595C>G MANE Select	ENSP00000262418.6:p.Leu865=
ENST00000262418.10:c.2595C>G	ENSP00000262418.6:p.Leu865=
ENST00000399246.3:c.1497C>G	ENSP00000382190.3:p.Leu499=
NM_000342.3:c.2595C>G	NP_000333.1:p.Leu865=
XM_005257593.3:c.2400C>G	XP_005257650.1:p.Leu800=
XM_011525129.1:c.2505C>G	XP_011523431.1:p.Leu835=
XM_005257593.5:c.2400C>G	XP_005257650.1:p.Leu800=
XM_011525129.2:c.2505C>G	XP_011523431.1:p.Leu835=
NM_000342.4:c.2595C>G MANE Select	NP_000333.1:p.Leu865=