Canonical Allele Identifier: CA376859239

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959237T>C (hg19) ; chr10:g.68199480T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199480T>C , CM000672.2:g.68199480T>C	GRCh38
NC_000010.10:g.69959237T>C , CM000672.1:g.69959237T>C	GRCh37
NC_000010.9:g.69629243T>C	NCBI36
NG_032118.1:g.98364T>C , LRG_410:g.98364T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2573T>C	ENSP00000346369.2:p.Ile858Thr
ENST00000540630.6:c.3452T>C	ENSP00000441668.3:p.Ile1151Thr
ENST00000613327.5:c.3398T>C	ENSP00000480757.2:p.Ile1133Thr
ENST00000688812.1:c.*661T>C	ENSP00000510658.1:n.*661T>C
ENST00000690544.1:c.*2669T>C	ENSP00000508989.1:n.*2669T>C
ENST00000358913.10:c.3398T>C MANE Select	ENSP00000351790.5:p.Ile1133Thr
ENST00000354393.6:c.2573T>C	ENSP00000346369.2:p.Ile858Thr
ENST00000358913.9:c.3398T>C	ENSP00000351790.5:p.Ile1133Thr
ENST00000540630.5:c.3398T>C	ENSP00000441668.2:p.Ile1133Thr
ENST00000613327.4:c.2516T>C	ENSP00000480757.1:p.Ile839Thr
NM_001256267.1:c.3398T>C	NP_001243196.1:p.Ile1133Thr
NM_001256268.1:c.2516T>C	NP_001243197.1:p.Ile839Thr
NM_032578.3:c.3398T>C , LRG_410t1:c.3398T>C	NP_115967.2:p.Ile1133Thr
NR_045662.3:n.2825T>C
NR_045663.3:n.3527T>C
XM_006718043.2:c.3452T>C	XP_006718106.1:p.Ile1151Thr
XM_011540292.1:c.3428T>C	XP_011538594.1:p.Ile1143Thr
XR_946029.1:n.1804-205A>G
XM_017016833.1:c.3476T>C	XP_016872322.1:p.Ile1159Thr
XM_017016834.2:c.3398T>C	XP_016872323.1:p.Ile1133Thr
XM_024448236.1:c.2276T>C	XP_024304004.1:p.Ile759Thr
NR_045662.4:n.2935T>C
NR_045663.4:n.3472T>C
NM_001256267.2:c.3398T>C	NP_001243196.1:p.Ile1133Thr
NM_001256268.2:c.2516T>C	NP_001243197.1:p.Ile839Thr
NM_032578.4:c.3398T>C MANE Select	NP_115967.2:p.Ile1133Thr