Canonical Allele Identifier: CA399783392

Gene: SLC4A1

Linked Data

• MyVariant Identifiers: chr17:g.42331995G>C (hg19) ; chr17:g.44254627G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254627G>C , CM000679.2:g.44254627G>C	GRCh38
NC_000017.10:g.42331995G>C , CM000679.1:g.42331995G>C	GRCh37
NC_000017.9:g.39687521G>C	NCBI36
NG_007498.1:g.18508C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.1926C>G MANE Select	ENSP00000262418.6:p.Asn642Lys
ENST00000262418.10:c.1926C>G	ENSP00000262418.6:p.Asn642Lys
ENST00000399246.3:c.828C>G	ENSP00000382190.3:p.Asn276Lys
NM_000342.3:c.1926C>G	NP_000333.1:p.Asn642Lys
XM_005257593.3:c.1731C>G	XP_005257650.1:p.Asn577Lys
XM_011525129.1:c.1836C>G	XP_011523431.1:p.Asn612Lys
XM_011525130.1:c.1926C>G	XP_011523432.1:p.Asn642Lys
XM_011525131.1:c.1926C>G	XP_011523433.1:p.Asn642Lys
XM_005257593.5:c.1731C>G	XP_005257650.1:p.Asn577Lys
XM_011525129.2:c.1836C>G	XP_011523431.1:p.Asn612Lys
NM_000342.4:c.1926C>G MANE Select	NP_000333.1:p.Asn642Lys