Canonical Allele Identifier: CA412400230

Gene: MAP3K15

Linked Data

• gnomAD v4: X-19362824-T-A
• MyVariant Identifiers: chrX:g.19380942T>A (hg19) ; chrX:g.19362824T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19362824T>A , CM000685.2:g.19362824T>A	GRCh38
NC_000023.10:g.19380942T>A , CM000685.1:g.19380942T>A	GRCh37
NC_000023.9:g.19290863T>A	NCBI36
NG_016781.1:g.23932T>A
NG_021184.1:g.157438A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338883.9:c.3593A>T MANE Select	ENSP00000345629.4:p.Glu1198Val
ENST00000338883.8:c.3593A>T	ENSP00000345629.4:p.Glu1198Val
ENST00000359173.7:c.2921A>T
ENST00000470101.1:n.1011A>T
ENST00000518578.5:n.3655A>T
NM_001001671.3:c.3593A>T	NP_001001671.3:p.Glu1198Val
XM_011545507.1:c.3248A>T	XP_011543809.1:p.Glu1083Val
XM_011545508.1:c.3161A>T	XP_011543810.1:p.Glu1054Val
XM_011545509.1:c.2558A>T	XP_011543811.1:p.Glu853Val
XM_011545510.1:c.2267A>T	XP_011543812.1:p.Glu756Val
XM_011545511.1:c.1898A>T	XP_011543813.1:p.Glu633Val
XM_011545507.3:c.3248A>T	XP_011543809.3:p.Glu1083Val
XM_011545508.3:c.3161A>T	XP_011543810.3:p.Glu1054Val
XM_011545510.2:c.2267A>T	XP_011543812.1:p.Glu756Val
XM_011545511.2:c.1898A>T	XP_011543813.1:p.Glu633Val
NM_001001671.4:c.3593A>T MANE Select	NP_001001671.3:p.Glu1198Val