Canonical Allele Identifier: CA381515647

Gene: CABP2

Linked Data

• MyVariant Identifiers: chr11:g.67288547G>T (hg19) ; chr11:g.67521076G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521076G>T , CM000673.2:g.67521076G>T	GRCh38
NC_000011.9:g.67288547G>T , CM000673.1:g.67288547G>T	GRCh37
NC_000011.8:g.67045123G>T	NCBI36
NG_032982.1:g.7353C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.328C>A MANE Select	ENSP00000294288.4:p.Leu110Met
ENST00000545205.2:c.*113C>A	ENSP00000446180.1:n.*113C>A
ENST00000636477.1:c.280C>A	ENSP00000490746.1:p.Leu94Met
ENST00000294288.4:c.328C>A	ENSP00000294288.4:p.Leu110Met
ENST00000353903.9:c.157C>A	ENSP00000312037.4:p.Leu53Met
ENST00000545205.1:c.*113C>A	ENSP00000446180.1:n.*113C>A
NM_016366.2:c.328C>A	NP_057450.2:p.Leu110Met
XM_005274046.1:c.346C>A	XP_005274103.1:p.Leu116Met
NM_001318496.1:c.346C>A	NP_001305425.1:p.Leu116Met
NM_001318496.2:c.346C>A	NP_001305425.1:p.Leu116Met
NM_016366.3:c.328C>A MANE Select	NP_057450.2:p.Leu110Met