Canonical Allele Identifier: CA376857228

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955206G>A (hg19) ; chr10:g.68195449G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195449G>A , CM000672.2:g.68195449G>A	GRCh38
NC_000010.10:g.69955206G>A , CM000672.1:g.69955206G>A	GRCh37
NC_000010.9:g.69625212G>A	NCBI36
NG_032118.1:g.94333G>A , LRG_410:g.94333G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.2251-1G>A	ENSP00000346369.2:n.2251-1G>A
ENST00000540630.6:c.3130-1G>A	ENSP00000441668.3:n.3130-1G>A
ENST00000613327.5:c.3076-1G>A	ENSP00000480757.2:n.3076-1G>A
ENST00000688812.1:c.*339-1G>A	ENSP00000510658.1:n.*339-1G>A
ENST00000690544.1:c.*2347-1G>A	ENSP00000508989.1:n.*2347-1G>A
ENST00000358913.10:c.3076-1G>A MANE Select	ENSP00000351790.5:n.3076-1G>A
ENST00000354393.6:c.2251-1G>A	ENSP00000346369.2:n.2251-1G>A
ENST00000358913.9:c.3076-1G>A	ENSP00000351790.5:n.3076-1G>A
ENST00000540630.5:c.3076-1G>A	ENSP00000441668.2:n.3076-1G>A
ENST00000613327.4:c.2194-1G>A	ENSP00000480757.1:n.2194-1G>A
NM_001256267.1:c.3076-1G>A	NP_001243196.1:n.3076-1G>A
NM_001256268.1:c.2194-1G>A	NP_001243197.1:n.2194-1G>A
NM_032578.3:c.3076-1G>A , LRG_410t1:c.3076-1G>A	NP_115967.2:n.3076-1G>A
NR_045662.3:n.2503-1G>A
NR_045663.3:n.3205-1G>A
XM_006718043.2:c.3130-1G>A	XP_006718106.1:n.3130-1G>A
XM_011540292.1:c.3106-1G>A	XP_011538594.1:n.3106-1G>A
XM_017016833.1:c.3154-1G>A	XP_016872322.1:n.3154-1G>A
XM_017016834.2:c.3076-1G>A	XP_016872323.1:n.3076-1G>A
XM_024448236.1:c.1954-1G>A	XP_024304004.1:n.1954-1G>A
NR_045662.4:n.2613-1G>A
NR_045663.4:n.3150-1G>A
NM_001256267.2:c.3076-1G>A	NP_001243196.1:n.3076-1G>A
NM_001256268.2:c.2194-1G>A	NP_001243197.1:n.2194-1G>A
NM_032578.4:c.3076-1G>A MANE Select	NP_115967.2:n.3076-1G>A