Canonical Allele Identifier: CA376858851

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959125G>C (hg19) ; chr10:g.68199368G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199368G>C , CM000672.2:g.68199368G>C	GRCh38
NC_000010.10:g.69959125G>C , CM000672.1:g.69959125G>C	GRCh37
NC_000010.9:g.69629131G>C	NCBI36
NG_032118.1:g.98252G>C , LRG_410:g.98252G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2461G>C	ENSP00000346369.2:p.Val821Leu
ENST00000540630.6:c.3340G>C	ENSP00000441668.3:p.Val1114Leu
ENST00000613327.5:c.3286G>C	ENSP00000480757.2:p.Val1096Leu
ENST00000688812.1:c.*549G>C	ENSP00000510658.1:n.*549G>C
ENST00000690544.1:c.*2557G>C	ENSP00000508989.1:n.*2557G>C
ENST00000358913.10:c.3286G>C MANE Select	ENSP00000351790.5:p.Val1096Leu
ENST00000354393.6:c.2461G>C	ENSP00000346369.2:p.Val821Leu
ENST00000358913.9:c.3286G>C	ENSP00000351790.5:p.Val1096Leu
ENST00000540630.5:c.3286G>C	ENSP00000441668.2:p.Val1096Leu
ENST00000613327.4:c.2404G>C	ENSP00000480757.1:p.Val802Leu
NM_001256267.1:c.3286G>C	NP_001243196.1:p.Val1096Leu
NM_001256268.1:c.2404G>C	NP_001243197.1:p.Val802Leu
NM_032578.3:c.3286G>C , LRG_410t1:c.3286G>C	NP_115967.2:p.Val1096Leu
NR_045662.3:n.2713G>C
NR_045663.3:n.3415G>C
XM_006718043.2:c.3340G>C	XP_006718106.1:p.Val1114Leu
XM_011540292.1:c.3316G>C	XP_011538594.1:p.Val1106Leu
XR_946029.1:n.1804-93C>G
XM_017016833.1:c.3364G>C	XP_016872322.1:p.Val1122Leu
XM_017016834.2:c.3286G>C	XP_016872323.1:p.Val1096Leu
XM_024448236.1:c.2164G>C	XP_024304004.1:p.Val722Leu
NR_045662.4:n.2823G>C
NR_045663.4:n.3360G>C
NM_001256267.2:c.3286G>C	NP_001243196.1:p.Val1096Leu
NM_001256268.2:c.2404G>C	NP_001243197.1:p.Val802Leu
NM_032578.4:c.3286G>C MANE Select	NP_115967.2:p.Val1096Leu