Canonical Allele Identifier: CA1232989893

Gene: ALKAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.279705C= , CM000664.2:g.279705C=	GRCh38
NC_000002.11:g.279705C= , CM000664.1:g.279705C=	GRCh37
NC_000002.10:g.269705C=	NCBI36
NG_012035.1:g.19837C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403610.9:c.*442G= MANE Select	ENSP00000384604.3:n.*442G=
ENST00000403610.8:c.*442G=	ENSP00000384604.3:n.*442G=
NM_001002919.2:c.*442G=	NP_001002919.2:n.*442G=
XM_005264689.3:c.*442G=	XP_005264746.1:n.*442G=
XM_006711879.2:c.*442G=	XP_006711942.1:n.*442G=
XM_006711881.2:c.*442G=	XP_006711944.1:n.*442G=
XM_011510342.1:c.*442G=	XP_011508644.1:n.*442G=
XM_005264689.5:c.*442G=	XP_005264746.1:n.*442G=
XM_006711879.4:c.*442G=	XP_006711942.1:n.*442G=
XM_011510342.3:c.*442G=	XP_011508644.1:n.*442G=
NM_001002919.3:c.*442G= MANE Select	NP_001002919.2:n.*442G=