Canonical Allele Identifier: CA376840432

Gene: MYPN

Linked Data

• gnomAD v4: 10-68166536-G-C
• MyVariant Identifiers: chr10:g.69926293G>C (hg19) ; chr10:g.68166536G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166536G>C , CM000672.2:g.68166536G>C	GRCh38
NC_000010.10:g.69926293G>C , CM000672.1:g.69926293G>C	GRCh37
NC_000010.9:g.69596299G>C	NCBI36
NG_032118.1:g.65420G>C , LRG_410:g.65420G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1018G>C	ENSP00000346369.2:p.Ala340Pro
ENST00000373675.4:c.1843G>C	ENSP00000362779.4:p.Ala615Pro
ENST00000540630.6:c.1897G>C	ENSP00000441668.3:p.Ala633Pro
ENST00000613327.5:c.1843G>C	ENSP00000480757.2:p.Ala615Pro
ENST00000687572.1:c.721G>C	ENSP00000510427.1:p.Ala241Pro
ENST00000688812.1:c.1819G>C	ENSP00000510658.1:p.Ala607Pro
ENST00000690544.1:c.*1114G>C	ENSP00000508989.1:n.*1114G>C
ENST00000358913.10:c.1843G>C MANE Select	ENSP00000351790.5:p.Ala615Pro
ENST00000354393.6:c.1018G>C	ENSP00000346369.2:p.Ala340Pro
ENST00000358913.9:c.1843G>C	ENSP00000351790.5:p.Ala615Pro
ENST00000540630.5:c.1843G>C	ENSP00000441668.2:p.Ala615Pro
ENST00000613327.4:c.961G>C	ENSP00000480757.1:p.Ala321Pro
NM_001256267.1:c.1843G>C	NP_001243196.1:p.Ala615Pro
NM_001256268.1:c.961G>C	NP_001243197.1:p.Ala321Pro
NM_032578.3:c.1843G>C , LRG_410t1:c.1843G>C	NP_115967.2:p.Ala615Pro
NR_045662.3:n.1270G>C
NR_045663.3:n.2111G>C
XM_006718043.2:c.1897G>C	XP_006718106.1:p.Ala633Pro
XM_011540292.1:c.1873G>C	XP_011538594.1:p.Ala625Pro
XM_017016833.1:c.1921G>C	XP_016872322.1:p.Ala641Pro
XM_017016834.2:c.1843G>C	XP_016872323.1:p.Ala615Pro
XM_024448236.1:c.721G>C	XP_024304004.1:p.Ala241Pro
NR_045662.4:n.1380G>C
NR_045663.4:n.2056G>C
NM_001256267.2:c.1843G>C	NP_001243196.1:p.Ala615Pro
NM_001256268.2:c.961G>C	NP_001243197.1:p.Ala321Pro
NM_032578.4:c.1843G>C MANE Select	NP_115967.2:p.Ala615Pro