Canonical Allele Identifier: CA1829677345

Gene: JAK2 MTATP6P11 INSL6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5099648T= , CM000671.2:g.5099648T=	GRCh38
NC_000009.11:g.5099648T= , CM000671.1:g.5099648T=	GRCh37
NC_000009.10:g.5089648T=	NCBI36
NG_009904.1:g.119404T= , LRG_612:g.119404T=
NG_046969.1:g.91063A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381652.4:c.3059+8737T= (JAK2) MANE Select	ENSP00000371067.4:n.3059+8737T=
ENST00000381652.3:c.3059+8737T= (JAK2)	ENSP00000371067.3:n.3059+8737T=
ENST00000428071.1:n.89T= (MTATP6P11)
NM_004972.3:c.3059+8737T= , LRG_612t1:c.3059+8737T= (JAK2)	NP_004963.1:n.3059+8737T=
XM_011517701.1:c.376+64531A= (INSL6)	XP_011516003.1:n.376+64531A=
XM_011517702.1:c.376+64531A= (INSL6)	XP_011516004.1:n.376+64531A=
XR_929169.1:n.484+64531A= (INSL6)
NM_001322194.1:c.3059+8737T= (JAK2)	NP_001309123.1:n.3059+8737T=
NM_001322195.1:c.3059+8737T= (JAK2)	NP_001309124.1:n.3059+8737T=
NM_001322196.1:c.3059+8737T= (JAK2)	NP_001309125.1:n.3059+8737T=
NM_001322198.1:c.1844+8737T= (JAK2)	NP_001309127.1:n.1844+8737T=
NM_001322199.1:c.1844+8737T= (JAK2)	NP_001309128.1:n.1844+8737T=
NM_001322204.1:c.2612+8737T= (JAK2)	NP_001309133.1:n.2612+8737T=
XM_011517702.3:c.376+64531A= (INSL6)	XP_011516004.1:n.376+64531A=
NM_004972.4:c.3059+8737T= (JAK2) MANE Select	NP_004963.1:n.3059+8737T=
NM_001322194.2:c.3059+8737T= (JAK2)	NP_001309123.1:n.3059+8737T=
NM_001322195.2:c.3059+8737T= (JAK2)	NP_001309124.1:n.3059+8737T=
NM_001322196.2:c.3059+8737T= (JAK2)	NP_001309125.1:n.3059+8737T=
NM_001322198.2:c.1844+8737T= (JAK2)	NP_001309127.1:n.1844+8737T=
NM_001322199.2:c.1844+8737T= (JAK2)	NP_001309128.1:n.1844+8737T=
NM_001322204.2:c.2612+8737T= (JAK2)	NP_001309133.1:n.2612+8737T=
NR_169763.1:n.3543+8737T= (JAK2)
NR_169764.1:n.3460+8737T= (JAK2)