Canonical Allele Identifier: CA1837882510

Gene: SLC24A2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.19579429G= , CM000671.2:g.19579429G=	GRCh38
NC_000009.11:g.19579427G= , CM000671.1:g.19579427G=	GRCh37
NC_000009.10:g.19569427G=	NCBI36
NG_029734.1:g.212591C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286344.4:c.1079-2407C=	ENSP00000286344.3:n.1079-2407C=
ENST00000341998.7:c.1130-2407C= MANE Select	ENSP00000344801.1:n.1130-2407C=
ENST00000286344.3:c.1079-2407C=	ENSP00000286344.3:n.1079-2407C=
ENST00000341998.6:c.1130-2407C=	ENSP00000344801.1:n.1130-2407C=
NM_001193288.2:c.1079-2407C=	NP_001180217.1:n.1079-2407C=
NM_020344.3:c.1130-2407C=	NP_065077.1:n.1130-2407C=
XM_005251425.1:c.1130-2407C=	XP_005251482.1:n.1130-2407C=
XM_005251426.3:c.1130-2407C=	XP_005251483.1:n.1130-2407C=
XM_006716750.2:c.1079-2407C=	XP_006716813.1:n.1079-2407C=
XM_005251425.2:c.1130-2407C=	XP_005251482.1:n.1130-2407C=
XM_005251426.4:c.1130-2407C=	XP_005251483.1:n.1130-2407C=
XM_006716750.4:c.1079-2407C=	XP_006716813.1:n.1079-2407C=
XM_017014592.1:c.1130-2407C=	XP_016870081.1:n.1130-2407C=
XM_017014593.1:c.1079-2407C=	XP_016870082.1:n.1079-2407C=
NM_001193288.3:c.1079-2407C=	NP_001180217.1:n.1079-2407C=
NM_001375850.1:c.1130-2407C=	NP_001362779.1:n.1130-2407C=
NM_001375851.1:c.1079-2407C=	NP_001362780.1:n.1079-2407C=
NM_020344.4:c.1130-2407C= MANE Select	NP_065077.1:n.1130-2407C=