Canonical Allele Identifier: CA376859237

Gene: MYPN

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2573T>A	ENSP00000346369.2:p.Ile858Asn
ENST00000540630.6:c.3452T>A	ENSP00000441668.3:p.Ile1151Asn
ENST00000613327.5:c.3398T>A	ENSP00000480757.2:p.Ile1133Asn
ENST00000688812.1:c.*661T>A	ENSP00000510658.1:n.*661T>A
ENST00000690544.1:c.*2669T>A	ENSP00000508989.1:n.*2669T>A
ENST00000358913.10:c.3398T>A MANE Select	ENSP00000351790.5:p.Ile1133Asn
ENST00000354393.6:c.2573T>A	ENSP00000346369.2:p.Ile858Asn
ENST00000358913.9:c.3398T>A	ENSP00000351790.5:p.Ile1133Asn
ENST00000540630.5:c.3398T>A	ENSP00000441668.2:p.Ile1133Asn
ENST00000613327.4:c.2516T>A	ENSP00000480757.1:p.Ile839Asn
NM_001256267.1:c.3398T>A	NP_001243196.1:p.Ile1133Asn
NM_001256268.1:c.2516T>A	NP_001243197.1:p.Ile839Asn
NM_032578.3:c.3398T>A , LRG_410t1:c.3398T>A	NP_115967.2:p.Ile1133Asn
NR_045662.3:n.2825T>A
NR_045663.3:n.3527T>A
XM_006718043.2:c.3452T>A	XP_006718106.1:p.Ile1151Asn
XM_011540292.1:c.3428T>A	XP_011538594.1:p.Ile1143Asn
XR_946029.1:n.1804-205A>T
XM_017016833.1:c.3476T>A	XP_016872322.1:p.Ile1159Asn
XM_017016834.2:c.3398T>A	XP_016872323.1:p.Ile1133Asn
XM_024448236.1:c.2276T>A	XP_024304004.1:p.Ile759Asn
NR_045662.4:n.2935T>A
NR_045663.4:n.3472T>A
NM_001256267.2:c.3398T>A	NP_001243196.1:p.Ile1133Asn
NM_001256268.2:c.2516T>A	NP_001243197.1:p.Ile839Asn
NM_032578.4:c.3398T>A MANE Select	NP_115967.2:p.Ile1133Asn