Canonical Allele Identifier: CA2609373527

Gene: MYPN

Linked Data

• gnomAD v4: 10-68199279-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199279T>C , CM000672.2:g.68199279T>C	GRCh38
NC_000010.10:g.69959036T>C , CM000672.1:g.69959036T>C	GRCh37
NC_000010.9:g.69629042T>C	NCBI36
NG_032118.1:g.98163T>C , LRG_410:g.98163T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2461-89T>C	ENSP00000346369.2:n.2461-89T>C
ENST00000540630.6:c.3340-89T>C	ENSP00000441668.3:n.3340-89T>C
ENST00000613327.5:c.3286-89T>C	ENSP00000480757.2:n.3286-89T>C
ENST00000688812.1:c.*549-89T>C	ENSP00000510658.1:n.*549-89T>C
ENST00000690544.1:c.*2557-89T>C	ENSP00000508989.1:n.*2557-89T>C
ENST00000358913.10:c.3286-89T>C MANE Select	ENSP00000351790.5:n.3286-89T>C
ENST00000354393.6:c.2461-89T>C	ENSP00000346369.2:n.2461-89T>C
ENST00000358913.9:c.3286-89T>C	ENSP00000351790.5:n.3286-89T>C
ENST00000540630.5:c.3286-89T>C	ENSP00000441668.2:n.3286-89T>C
ENST00000613327.4:c.2404-89T>C	ENSP00000480757.1:n.2404-89T>C
NM_001256267.1:c.3286-89T>C	NP_001243196.1:n.3286-89T>C
NM_001256268.1:c.2404-89T>C	NP_001243197.1:n.2404-89T>C
NM_032578.3:c.3286-89T>C , LRG_410t1:c.3286-89T>C	NP_115967.2:n.3286-89T>C
NR_045662.3:n.2713-89T>C
NR_045663.3:n.3415-89T>C
XM_006718043.2:c.3340-89T>C	XP_006718106.1:n.3340-89T>C
XM_011540292.1:c.3316-89T>C	XP_011538594.1:n.3316-89T>C
XR_946029.1:n.1804-4A>G
XM_017016833.1:c.3364-89T>C	XP_016872322.1:n.3364-89T>C
XM_017016834.2:c.3286-89T>C	XP_016872323.1:n.3286-89T>C
XM_024448236.1:c.2164-89T>C	XP_024304004.1:n.2164-89T>C
NR_045662.4:n.2823-89T>C
NR_045663.4:n.3360-89T>C
NM_001256267.2:c.3286-89T>C	NP_001243196.1:n.3286-89T>C
NM_001256268.2:c.2404-89T>C	NP_001243197.1:n.2404-89T>C
NM_032578.4:c.3286-89T>C MANE Select	NP_115967.2:n.3286-89T>C