Canonical Allele Identifier: CA439875650

Gene: SLC4A4

Linked Data

• MyVariant Identifiers: chr4:g.72316977A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71451260A>G , CM000666.2:g.71451260A>G	GRCh38
NC_000004.11:g.72316977A>G , CM000666.1:g.72316977A>G	GRCh37
NC_000004.10:g.72535841A>G	NCBI36
NG_012653.1:g.268975A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698522.1:c.1377A>G	ENSP00000513771.1:p.Gly459=
ENST00000264485.11:c.1281A>G MANE Select	ENSP00000264485.5:p.Gly427=
ENST00000340595.4:c.1149A>G MANE Plus Clinical	ENSP00000344272.3:p.Gly383=
ENST00000649996.1:c.1281A>G	ENSP00000497468.1:p.Gly427=
ENST00000264485.9:c.1281A>G	ENSP00000264485.5:p.Gly427=
ENST00000340595.3:c.1149A>G	ENSP00000344272.3:p.Gly383=
ENST00000351898.10:c.1281A>G	ENSP00000307349.7:p.Gly427=
ENST00000425175.5:c.1281A>G	ENSP00000393557.1:p.Gly427=
ENST00000512686.5:c.1149A>G	ENSP00000422400.1:p.Gly383=
ENST00000514331.1:n.1210A>G
NM_001098484.2:c.1281A>G	NP_001091954.1:p.Gly427=
NM_001134742.1:c.1281A>G	NP_001128214.1:p.Gly427=
NM_003759.3:c.1149A>G	NP_003750.1:p.Gly383=
XM_011532390.1:c.723A>G	XP_011530692.1:p.Gly241=
XM_011532390.2:c.723A>G	XP_011530692.1:p.Gly241=
XM_017008792.1:c.1056A>G	XP_016864281.1:p.Gly352=
XM_017008793.1:c.765A>G	XP_016864282.1:p.Gly255=
XM_024454267.1:c.1374A>G	XP_024310035.1:p.Gly458=
XM_024454268.1:c.1296A>G	XP_024310036.1:p.Gly432=
XM_024454269.1:c.1296A>G	XP_024310037.1:p.Gly432=
XM_024454270.1:c.1281A>G	XP_024310038.1:p.Gly427=
XM_024454271.1:c.1281A>G	XP_024310039.1:p.Gly427=
XM_024454272.1:c.1281A>G	XP_024310040.1:p.Gly427=
NM_001098484.3:c.1281A>G MANE Select	NP_001091954.1:p.Gly427=
NM_001134742.2:c.1281A>G	NP_001128214.1:p.Gly427=
NM_003759.4:c.1149A>G MANE Plus Clinical	NP_003750.1:p.Gly383=