Canonical Allele Identifier: CA2640134816

Gene: BIRC5

Linked Data

• gnomAD v4: 17-78224073-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224073_78224074insA , CM000679.2:g.78224073_78224074insA	GRCh38
NC_000017.10:g.76220154_76220155insA , CM000679.1:g.76220154_76220155insA	GRCh37
NC_000017.9:g.73731749_73731750insA	NCBI36
NG_029069.1:g.14878_14879insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*519_*520insA MANE Select	ENSP00000324180.4:n.*519_*520insA
ENST00000301633.8:c.*519_*520insA	ENSP00000301633.3:n.*519_*520insA
ENST00000350051.7:c.*519_*520insA	ENSP00000324180.4:n.*519_*520insA
ENST00000374948.6:c.*416_*417insA	ENSP00000364086.1:n.*416_*417insA
NM_001012270.1:c.*416_*417insA	NP_001012270.1:n.*416_*417insA
NM_001012271.1:c.*519_*520insA	NP_001012271.1:n.*519_*520insA
NM_001168.2:c.*519_*520insA	NP_001159.2:n.*519_*520insA
XR_243654.3:n.1150_1151insA
XR_934452.1:n.1219_1220insA
XR_243654.5:n.1150_1151insA
XR_934452.3:n.1219_1220insA
NM_001168.3:c.*519_*520insA MANE Select	NP_001159.2:n.*519_*520insA
NM_001012270.2:c.*416_*417insA	NP_001012270.1:n.*416_*417insA
NM_001012271.2:c.*519_*520insA	NP_001012271.1:n.*519_*520insA