Canonical Allele Identifier: CA208222722

Gene: MYPN

Linked Data

• dbSNP Id: rs564535893
• gnomAD v2: 10-69955121-C-T
• gnomAD v3: 10-68195364-C-T
• gnomAD v4: 10-68195364-C-T
• MyVariant Identifiers: chr10:g.69955121C>T (hg19) ; chr10:g.68195364C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195364C>T , CM000672.2:g.68195364C>T	GRCh38
NC_000010.10:g.69955121C>T , CM000672.1:g.69955121C>T	GRCh37
NC_000010.9:g.69625127C>T	NCBI36
NG_032118.1:g.94248C>T , LRG_410:g.94248C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.2251-86C>T	ENSP00000346369.2:n.2251-86C>T
ENST00000540630.6:c.3130-86C>T	ENSP00000441668.3:n.3130-86C>T
ENST00000613327.5:c.3076-86C>T	ENSP00000480757.2:n.3076-86C>T
ENST00000688812.1:c.*339-86C>T	ENSP00000510658.1:n.*339-86C>T
ENST00000690544.1:c.*2347-86C>T	ENSP00000508989.1:n.*2347-86C>T
ENST00000358913.10:c.3076-86C>T MANE Select	ENSP00000351790.5:n.3076-86C>T
ENST00000354393.6:c.2251-86C>T	ENSP00000346369.2:n.2251-86C>T
ENST00000358913.9:c.3076-86C>T	ENSP00000351790.5:n.3076-86C>T
ENST00000540630.5:c.3076-86C>T	ENSP00000441668.2:n.3076-86C>T
ENST00000613327.4:c.2194-86C>T	ENSP00000480757.1:n.2194-86C>T
NM_001256267.1:c.3076-86C>T	NP_001243196.1:n.3076-86C>T
NM_001256268.1:c.2194-86C>T	NP_001243197.1:n.2194-86C>T
NM_032578.3:c.3076-86C>T , LRG_410t1:c.3076-86C>T	NP_115967.2:n.3076-86C>T
NR_045662.3:n.2503-86C>T
NR_045663.3:n.3205-86C>T
XM_006718043.2:c.3130-86C>T	XP_006718106.1:n.3130-86C>T
XM_011540292.1:c.3106-86C>T	XP_011538594.1:n.3106-86C>T
XM_017016833.1:c.3154-86C>T	XP_016872322.1:n.3154-86C>T
XM_017016834.2:c.3076-86C>T	XP_016872323.1:n.3076-86C>T
XM_024448236.1:c.1954-86C>T	XP_024304004.1:n.1954-86C>T
NR_045662.4:n.2613-86C>T
NR_045663.4:n.3150-86C>T
NM_001256267.2:c.3076-86C>T	NP_001243196.1:n.3076-86C>T
NM_001256268.2:c.2194-86C>T	NP_001243197.1:n.2194-86C>T
NM_032578.4:c.3076-86C>T MANE Select	NP_115967.2:n.3076-86C>T