Canonical Allele Identifier: CA772089353

Gene: STAT5B

Linked Data

• dbSNP Id: rs1272200251
• gnomAD v3: 17-42261918-TCGAACTCC-T
• gnomAD v4: 17-42261918-TCGAACTCC-T
• MyVariant Identifiers: chr17:g.40413937_40413944del (hg19) ; chr17:g.42261919_42261926del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42261921_42261928del , CM000679.2:g.42261921_42261928del	GRCh38
NC_000017.10:g.40413939_40413946del , CM000679.1:g.40413939_40413946del	GRCh37
NC_000017.9:g.37667465_37667472del	NCBI36
NG_007271.1:g.19481_19488del , LRG_192:g.19481_19488del

Transcript Alleles

HGVS	Amino-acid change
ENST00000415845.2:c.-11+14702_-11+14709del	ENSP00000398379.2:n.-11+14702_-11+14709del
ENST00000698774.1:n.164+14322_164+14329del
ENST00000698775.1:c.-11+14322_-11+14329del	ENSP00000513922.1:n.-11+14322_-11+14329del
ENST00000698776.1:c.-11+25861_-11+25868del	ENSP00000513923.1:n.-11+25861_-11+25868del
ENST00000698777.1:c.-11+26534_-11+26541del	ENSP00000513924.1:n.-11+26534_-11+26541del
ENST00000698778.1:c.-11+14322_-11+14329del	ENSP00000513925.1:n.-11+14322_-11+14329del
ENST00000698779.1:c.-11+14322_-11+14329del	ENSP00000513926.1:n.-11+14322_-11+14329del
ENST00000698803.1:c.-11+14322_-11+14329del	ENSP00000513945.1:n.-11+14322_-11+14329del
ENST00000698804.1:n.109+14322_109+14329del
ENST00000698805.1:n.111+14322_111+14329del
ENST00000698806.1:c.-11+14322_-11+14329del	ENSP00000513946.1:n.-11+14322_-11+14329del
ENST00000698807.1:n.144+14322_144+14329del
ENST00000698808.1:c.-11+14322_-11+14329del	ENSP00000513947.1:n.-11+14322_-11+14329del
ENST00000698809.1:c.-11+14322_-11+14329del	ENSP00000513948.1:n.-11+14322_-11+14329del
ENST00000698810.1:c.-11+14322_-11+14329del	ENSP00000513949.1:n.-11+14322_-11+14329del
ENST00000698813.1:c.-11+14322_-11+14329del	ENSP00000513951.1:n.-11+14322_-11+14329del
ENST00000698814.1:c.-11+14322_-11+14329del	ENSP00000513952.1:n.-11+14322_-11+14329del
ENST00000698815.1:c.-11+14322_-11+14329del	ENSP00000513953.1:n.-11+14322_-11+14329del
ENST00000698816.1:n.78+14322_78+14329del
ENST00000293328.8:c.-11+14322_-11+14329del MANE Select	ENSP00000293328.3:n.-11+14322_-11+14329del
ENST00000293328.7:c.-11+14322_-11+14329del	ENSP00000293328.3:n.-11+14322_-11+14329del
ENST00000415845.1:c.-11+14702_-11+14709del	ENSP00000398379.1:n.-11+14702_-11+14709del
ENST00000468312.1:n.159+14322_159+14329del
NM_012448.3:c.-11+14322_-11+14329del , LRG_192t1:c.-11+14322_-11+14329del	NP_036580.2:n.-11+14322_-11+14329del
XM_005257626.3:c.-11+14322_-11+14329del	XP_005257683.1:n.-11+14322_-11+14329del
XM_005257626.4:c.-11+14322_-11+14329del	XP_005257683.1:n.-11+14322_-11+14329del
XM_017024977.1:c.-136+14322_-136+14329del	XP_016880466.1:n.-136+14322_-136+14329del
XM_024450897.1:c.-11+25861_-11+25868del	XP_024306665.1:n.-11+25861_-11+25868del
XM_024450898.1:c.-11+6360_-11+6367del	XP_024306666.1:n.-11+6360_-11+6367del
NM_012448.4:c.-11+14322_-11+14329del MANE Select	NP_036580.2:n.-11+14322_-11+14329del