Canonical Allele Identifier: CA628014624

Gene: BIRC5

Linked Data

• dbSNP Id: rs1307344349
• gnomAD v2: 17-76220158-TG-T
• gnomAD v3: 17-78224077-TG-T
• gnomAD v4: 17-78224077-TG-T
• MyVariant Identifiers: chr17:g.76220159del (hg19) ; chr17:g.78224078del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224079del , CM000679.2:g.78224079del	GRCh38
NC_000017.10:g.76220160del , CM000679.1:g.76220160del	GRCh37
NC_000017.9:g.73731755del	NCBI36
NG_029069.1:g.14884del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*525del MANE Select	ENSP00000324180.4:n.*525del
ENST00000301633.8:c.*525del	ENSP00000301633.3:n.*525del
ENST00000350051.7:c.*525del	ENSP00000324180.4:n.*525del
ENST00000374948.6:c.*422del	ENSP00000364086.1:n.*422del
NM_001012270.1:c.*422del	NP_001012270.1:n.*422del
NM_001012271.1:c.*525del	NP_001012271.1:n.*525del
NM_001168.2:c.*525del	NP_001159.2:n.*525del
XR_243654.3:n.1156del
XR_934452.1:n.1225del
XR_243654.5:n.1156del
XR_934452.3:n.1225del
NM_001168.3:c.*525del MANE Select	NP_001159.2:n.*525del
NM_001012270.2:c.*422del	NP_001012270.1:n.*422del
NM_001012271.2:c.*525del	NP_001012271.1:n.*525del