Canonical Allele Identifier: CA381520471
Gene: CABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67523324C>T , CM000673.2:g.67523324C>T GRCh38
NC_000011.9:g.67290795C>T , CM000673.1:g.67290795C>T GRCh37
NC_000011.8:g.67047371C>T NCBI36
NG_032982.1:g.5105G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000294288.5:c.3G>A MANE Select ENSP00000294288.4:p.Met1Ile
ENST00000545205.2:c.3G>A ENSP00000446180.1:p.Met1Ile
ENST00000636477.1:c.165+888G>A ENSP00000490746.1:n.165+888G>A
ENST00000294288.4:c.3G>A ENSP00000294288.4:p.Met1Ile
ENST00000353903.9:c.3G>A ENSP00000312037.4:p.Met1Ile
ENST00000545205.1:c.3G>A ENSP00000446180.1:p.Met1Ile
NM_016366.2:c.3G>A NP_057450.2:p.Met1Ile
XM_005274046.1:c.17G>A XP_005274103.1:p.Trp6Ter
NM_001318496.1:c.17G>A NP_001305425.1:p.Trp6Ter
NM_001318496.2:c.17G>A NP_001305425.1:p.Trp6Ter
NM_016366.3:c.3G>A MANE Select NP_057450.2:p.Met1Ile