Canonical Allele Identifier: CA2609373088

Gene: MYPN

Linked Data

• gnomAD v4: 10-68195363-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195363A>C , CM000672.2:g.68195363A>C	GRCh38
NC_000010.10:g.69955120A>C , CM000672.1:g.69955120A>C	GRCh37
NC_000010.9:g.69625126A>C	NCBI36
NG_032118.1:g.94247A>C , LRG_410:g.94247A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.2251-87A>C	ENSP00000346369.2:n.2251-87A>C
ENST00000540630.6:c.3130-87A>C	ENSP00000441668.3:n.3130-87A>C
ENST00000613327.5:c.3076-87A>C	ENSP00000480757.2:n.3076-87A>C
ENST00000688812.1:c.*339-87A>C	ENSP00000510658.1:n.*339-87A>C
ENST00000690544.1:c.*2347-87A>C	ENSP00000508989.1:n.*2347-87A>C
ENST00000358913.10:c.3076-87A>C MANE Select	ENSP00000351790.5:n.3076-87A>C
ENST00000354393.6:c.2251-87A>C	ENSP00000346369.2:n.2251-87A>C
ENST00000358913.9:c.3076-87A>C	ENSP00000351790.5:n.3076-87A>C
ENST00000540630.5:c.3076-87A>C	ENSP00000441668.2:n.3076-87A>C
ENST00000613327.4:c.2194-87A>C	ENSP00000480757.1:n.2194-87A>C
NM_001256267.1:c.3076-87A>C	NP_001243196.1:n.3076-87A>C
NM_001256268.1:c.2194-87A>C	NP_001243197.1:n.2194-87A>C
NM_032578.3:c.3076-87A>C , LRG_410t1:c.3076-87A>C	NP_115967.2:n.3076-87A>C
NR_045662.3:n.2503-87A>C
NR_045663.3:n.3205-87A>C
XM_006718043.2:c.3130-87A>C	XP_006718106.1:n.3130-87A>C
XM_011540292.1:c.3106-87A>C	XP_011538594.1:n.3106-87A>C
XM_017016833.1:c.3154-87A>C	XP_016872322.1:n.3154-87A>C
XM_017016834.2:c.3076-87A>C	XP_016872323.1:n.3076-87A>C
XM_024448236.1:c.1954-87A>C	XP_024304004.1:n.1954-87A>C
NR_045662.4:n.2613-87A>C
NR_045663.4:n.3150-87A>C
NM_001256267.2:c.3076-87A>C	NP_001243196.1:n.3076-87A>C
NM_001256268.2:c.2194-87A>C	NP_001243197.1:n.2194-87A>C
NM_032578.4:c.3076-87A>C MANE Select	NP_115967.2:n.3076-87A>C