Canonical Allele Identifier: CA1917227432

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199513_68199514delinsAT , CM000672.2:g.68199513_68199514delinsAT	GRCh38
NC_000010.10:g.69959270_69959271delinsAT , CM000672.1:g.69959270_69959271delinsAT	GRCh37
NC_000010.9:g.69629276_69629277delinsAT	NCBI36
NG_032118.1:g.98397_98398delinsAT , LRG_410:g.98397_98398delinsAT

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3431_3432delinsAT MANE Select	NP_115967.2:p.Tyr1144=
ENST00000358913.10:c.3431_3432delinsAT MANE Select	ENSP00000351790.5:p.Tyr1144=
NM_001256267.1:c.3431_3432delinsAT	NP_001243196.1:p.Tyr1144=
NM_001256267.2:c.3431_3432delinsAT	NP_001243196.1:p.Tyr1144=
NM_001256268.1:c.2549_2550delinsAT	NP_001243197.1:p.Tyr850=
NM_001256268.2:c.2549_2550delinsAT	NP_001243197.1:p.Tyr850=
NM_032578.3:c.3431_3432delinsAT , LRG_410t1:c.3431_3432delinsAT	NP_115967.2:p.Tyr1144=
NR_045662.3:n.2858_2859delinsAT
NR_045662.4:n.2968_2969delinsAT
NR_045663.3:n.3560_3561delinsAT
NR_045663.4:n.3505_3506delinsAT
ENST00000354393.6:c.2606_2607delinsAT	ENSP00000346369.2:p.Tyr869=
ENST00000354393.7:c.2606_2607delinsAT	ENSP00000346369.2:p.Tyr869=
ENST00000358913.9:c.3431_3432delinsAT	ENSP00000351790.5:p.Tyr1144=
ENST00000540630.5:c.3431_3432delinsAT	ENSP00000441668.2:p.Tyr1144=
ENST00000540630.6:c.3485_3486delinsAT	ENSP00000441668.3:p.Tyr1162=
ENST00000613327.4:c.2549_2550delinsAT	ENSP00000480757.1:p.Tyr850=
ENST00000613327.5:c.3431_3432delinsAT	ENSP00000480757.2:p.Tyr1144=
ENST00000688812.1:c.*694_*695delinsAT	ENSP00000510658.1:n.*694_*695delinsAT
ENST00000690544.1:c.*2702_*2703delinsAT	ENSP00000508989.1:n.*2702_*2703delinsAT
XM_006718043.2:c.3485_3486delinsAT	XP_006718106.1:p.Tyr1162=
XM_011540292.1:c.3461_3462delinsAT	XP_011538594.1:p.Tyr1154=
XM_017016833.1:c.3509_3510delinsAT	XP_016872322.1:p.Tyr1170=
XM_017016834.2:c.3431_3432delinsAT	XP_016872323.1:p.Tyr1144=
XM_024448236.1:c.2309_2310delinsAT	XP_024304004.1:p.Tyr770=
XR_946029.1:n.1804-239_1804-238delinsAT