Canonical Allele Identifier: CA2609373330

Gene: MYPN

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68197278T>C , CM000672.2:g.68197278T>C	GRCh38
NC_000010.10:g.69957035T>C , CM000672.1:g.69957035T>C	GRCh37
NC_000010.9:g.69627041T>C	NCBI36
NG_032118.1:g.96162T>C , LRG_410:g.96162T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2334-74T>C	ENSP00000346369.2:n.2334-74T>C
ENST00000540630.6:c.3213-74T>C	ENSP00000441668.3:n.3213-74T>C
ENST00000613327.5:c.3159-74T>C	ENSP00000480757.2:n.3159-74T>C
ENST00000688812.1:c.*422-74T>C	ENSP00000510658.1:n.*422-74T>C
ENST00000690544.1:c.*2430-74T>C	ENSP00000508989.1:n.*2430-74T>C
ENST00000358913.10:c.3159-74T>C MANE Select	ENSP00000351790.5:n.3159-74T>C
ENST00000354393.6:c.2334-74T>C	ENSP00000346369.2:n.2334-74T>C
ENST00000358913.9:c.3159-74T>C	ENSP00000351790.5:n.3159-74T>C
ENST00000540630.5:c.3159-74T>C	ENSP00000441668.2:n.3159-74T>C
ENST00000613327.4:c.2277-74T>C	ENSP00000480757.1:n.2277-74T>C
NM_001256267.1:c.3159-74T>C	NP_001243196.1:n.3159-74T>C
NM_001256268.1:c.2277-74T>C	NP_001243197.1:n.2277-74T>C
NM_032578.3:c.3159-74T>C , LRG_410t1:c.3159-74T>C	NP_115967.2:n.3159-74T>C
NR_045662.3:n.2586-74T>C
NR_045663.3:n.3288-74T>C
XM_006718043.2:c.3213-74T>C	XP_006718106.1:n.3213-74T>C
XM_011540292.1:c.3189-74T>C	XP_011538594.1:n.3189-74T>C
XM_017016833.1:c.3237-74T>C	XP_016872322.1:n.3237-74T>C
XM_017016834.2:c.3159-74T>C	XP_016872323.1:n.3159-74T>C
XM_024448236.1:c.2037-74T>C	XP_024304004.1:n.2037-74T>C
NR_045662.4:n.2696-74T>C
NR_045663.4:n.3233-74T>C
NM_001256267.2:c.3159-74T>C	NP_001243196.1:n.3159-74T>C
NM_001256268.2:c.2277-74T>C	NP_001243197.1:n.2277-74T>C
NM_032578.4:c.3159-74T>C MANE Select	NP_115967.2:n.3159-74T>C