Canonical Allele Identifier: CA381515242

Gene: CABP2

Linked Data

• MyVariant Identifiers: chr11:g.67288496T>C (hg19) ; chr11:g.67521025T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521025T>C , CM000673.2:g.67521025T>C	GRCh38
NC_000011.9:g.67288496T>C , CM000673.1:g.67288496T>C	GRCh37
NC_000011.8:g.67045072T>C	NCBI36
NG_032982.1:g.7404A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.379A>G MANE Select	ENSP00000294288.4:p.Ser127Gly
ENST00000545205.2:c.*164A>G	ENSP00000446180.1:n.*164A>G
ENST00000636477.1:c.331A>G	ENSP00000490746.1:p.Ser111Gly
ENST00000294288.4:c.379A>G	ENSP00000294288.4:p.Ser127Gly
ENST00000353903.9:c.208A>G	ENSP00000312037.4:p.Ser70Gly
ENST00000545205.1:c.*164A>G	ENSP00000446180.1:n.*164A>G
NM_016366.2:c.379A>G	NP_057450.2:p.Ser127Gly
XM_005274046.1:c.397A>G	XP_005274103.1:p.Ser133Gly
NM_001318496.1:c.397A>G	NP_001305425.1:p.Ser133Gly
NM_001318496.2:c.397A>G	NP_001305425.1:p.Ser133Gly
NM_016366.3:c.379A>G MANE Select	NP_057450.2:p.Ser127Gly