Canonical Allele Identifier: CA1232989894
Gene: ALKAL2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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