Canonical Allele Identifier: CA10363380

Gene: MAP3K15

Linked Data

• dbSNP Id: rs764208000
• ExAC: X:19380880 G / C
• gnomAD v2: X-19380880-G-C
• gnomAD v4: X-19362762-G-C
• MyVariant Identifiers: chrX:g.19380880G>C (hg19) ; chrX:g.19362762G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19362762G>C , CM000685.2:g.19362762G>C	GRCh38
NC_000023.10:g.19380880G>C , CM000685.1:g.19380880G>C	GRCh37
NC_000023.9:g.19290801G>C	NCBI36
NG_016781.1:g.23870G>C
NG_021184.1:g.157500C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338883.9:c.3655C>G MANE Select	ENSP00000345629.4:p.Leu1219Val
ENST00000338883.8:c.3655C>G	ENSP00000345629.4:p.Leu1219Val
ENST00000359173.7:c.2983C>G
ENST00000470101.1:n.1073C>G
ENST00000518578.5:n.3717C>G
NM_001001671.3:c.3655C>G	NP_001001671.3:p.Leu1219Val
XM_011545507.1:c.3310C>G	XP_011543809.1:p.Leu1104Val
XM_011545508.1:c.3223C>G	XP_011543810.1:p.Leu1075Val
XM_011545509.1:c.2620C>G	XP_011543811.1:p.Leu874Val
XM_011545510.1:c.2329C>G	XP_011543812.1:p.Leu777Val
XM_011545511.1:c.1960C>G	XP_011543813.1:p.Leu654Val
XM_011545507.3:c.3310C>G	XP_011543809.3:p.Leu1104Val
XM_011545508.3:c.3223C>G	XP_011543810.3:p.Leu1075Val
XM_011545510.2:c.2329C>G	XP_011543812.1:p.Leu777Val
XM_011545511.2:c.1960C>G	XP_011543813.1:p.Leu654Val
NM_001001671.4:c.3655C>G MANE Select	NP_001001671.3:p.Leu1219Val