Canonical Allele Identifier: CA1829657900

Gene: JAK2 INSL6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5089726C= , CM000671.2:g.5089726C=	GRCh38
NC_000009.11:g.5089726C= , CM000671.1:g.5089726C=	GRCh37
NC_000009.10:g.5079726C=	NCBI36
NG_009904.1:g.109482C= , LRG_612:g.109482C=
NG_046969.1:g.100985G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381652.4:c.2624C= (JAK2) MANE Select	ENSP00000371067.4:p.Thr875=
ENST00000381652.3:c.2624C= (JAK2)	ENSP00000371067.3:p.Thr875=
NM_004972.3:c.2624C= , LRG_612t1:c.2624C= (JAK2)	NP_004963.1:p.Thr875=
XM_011517701.1:c.377-74382G= (INSL6)	XP_011516003.1:n.377-74382G=
XM_011517702.1:c.376+74453G= (INSL6)	XP_011516004.1:n.376+74453G=
XR_929169.1:n.485-74382G= (INSL6)
NM_001322194.1:c.2624C= (JAK2)	NP_001309123.1:p.Thr875=
NM_001322195.1:c.2624C= (JAK2)	NP_001309124.1:p.Thr875=
NM_001322196.1:c.2624C= (JAK2)	NP_001309125.1:p.Thr875=
NM_001322198.1:c.1409C= (JAK2)	NP_001309127.1:p.Thr470=
NM_001322199.1:c.1409C= (JAK2)	NP_001309128.1:p.Thr470=
NM_001322204.1:c.2177C= (JAK2)	NP_001309133.1:p.Thr726=
XM_011517702.3:c.376+74453G= (INSL6)	XP_011516004.1:n.376+74453G=
NM_004972.4:c.2624C= (JAK2) MANE Select	NP_004963.1:p.Thr875=
NM_001322194.2:c.2624C= (JAK2)	NP_001309123.1:p.Thr875=
NM_001322195.2:c.2624C= (JAK2)	NP_001309124.1:p.Thr875=
NM_001322196.2:c.2624C= (JAK2)	NP_001309125.1:p.Thr875=
NM_001322198.2:c.1409C= (JAK2)	NP_001309127.1:p.Thr470=
NM_001322199.2:c.1409C= (JAK2)	NP_001309128.1:p.Thr470=
NM_001322204.2:c.2177C= (JAK2)	NP_001309133.1:p.Thr726=
NR_169763.1:n.3108C= (JAK2)
NR_169764.1:n.3025C= (JAK2)