Canonical Allele Identifier: CA475382680

Gene: CABP2

Linked Data

• MyVariant Identifiers: chr11:g.67288542G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521071G>C , CM000673.2:g.67521071G>C	GRCh38
NC_000011.9:g.67288542G>C , CM000673.1:g.67288542G>C	GRCh37
NC_000011.8:g.67045118G>C	NCBI36
NG_032982.1:g.7358C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.333C>G MANE Select	ENSP00000294288.4:p.Gly111=
ENST00000545205.2:c.*118C>G	ENSP00000446180.1:n.*118C>G
ENST00000636477.1:c.285C>G	ENSP00000490746.1:p.Gly95=
ENST00000294288.4:c.333C>G	ENSP00000294288.4:p.Gly111=
ENST00000353903.9:c.162C>G	ENSP00000312037.4:p.Gly54=
ENST00000545205.1:c.*118C>G	ENSP00000446180.1:n.*118C>G
NM_016366.2:c.333C>G	NP_057450.2:p.Gly111=
XM_005274046.1:c.351C>G	XP_005274103.1:p.Gly117=
NM_001318496.1:c.351C>G	NP_001305425.1:p.Gly117=
NM_001318496.2:c.351C>G	NP_001305425.1:p.Gly117=
NM_016366.3:c.333C>G MANE Select	NP_057450.2:p.Gly111=