Canonical Allele Identifier: CA1467213295

Gene: SLC4A4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71451239C= , CM000666.2:g.71451239C=	GRCh38
NC_000004.11:g.72316956C= , CM000666.1:g.72316956C=	GRCh37
NC_000004.10:g.72535820C=	NCBI36
NG_012653.1:g.268954C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001098484.3:c.1260C= MANE Select	NP_001091954.1:p.Pro420=
ENST00000264485.11:c.1260C= MANE Select	ENSP00000264485.5:p.Pro420=
NM_003759.4:c.1128C= MANE Plus Clinical	NP_003750.1:p.Pro376=
ENST00000340595.4:c.1128C= MANE Plus Clinical	ENSP00000344272.3:p.Pro376=
NM_001098484.2:c.1260C=	NP_001091954.1:p.Pro420=
NM_001134742.1:c.1260C=	NP_001128214.1:p.Pro420=
NM_001134742.2:c.1260C=	NP_001128214.1:p.Pro420=
NM_003759.3:c.1128C=	NP_003750.1:p.Pro376=
ENST00000264485.9:c.1260C=	ENSP00000264485.5:p.Pro420=
ENST00000340595.3:c.1128C=	ENSP00000344272.3:p.Pro376=
ENST00000351898.10:c.1260C=	ENSP00000307349.7:p.Pro420=
ENST00000425175.5:c.1260C=	ENSP00000393557.1:p.Pro420=
ENST00000512686.5:c.1128C=	ENSP00000422400.1:p.Pro376=
ENST00000514331.1:n.1189C=
ENST00000649996.1:c.1260C=	ENSP00000497468.1:p.Pro420=
ENST00000698522.1:c.1356C=	ENSP00000513771.1:p.Pro452=
XM_011532390.1:c.702C=	XP_011530692.1:p.Pro234=
XM_011532390.2:c.702C=	XP_011530692.1:p.Pro234=
XM_017008792.1:c.1035C=	XP_016864281.1:p.Pro345=
XM_017008793.1:c.744C=	XP_016864282.1:p.Pro248=
XM_024454267.1:c.1353C=	XP_024310035.1:p.Pro451=
XM_024454268.1:c.1275C=	XP_024310036.1:p.Pro425=
XM_024454269.1:c.1275C=	XP_024310037.1:p.Pro425=
XM_024454270.1:c.1260C=	XP_024310038.1:p.Pro420=
XM_024454271.1:c.1260C=	XP_024310039.1:p.Pro420=
XM_024454272.1:c.1260C=	XP_024310040.1:p.Pro420=