Canonical Allele Identifier: CA2693252659

Gene: MAP3K15

Linked Data

• gnomAD v4: X-19362861-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19362861A>T , CM000685.2:g.19362861A>T	GRCh38
NC_000023.10:g.19380979A>T , CM000685.1:g.19380979A>T	GRCh37
NC_000023.9:g.19290900A>T	NCBI36
NG_016781.1:g.23969A>T
NG_021184.1:g.157401T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338883.9:c.3567-11T>A MANE Select	ENSP00000345629.4:n.3567-11T>A
ENST00000338883.8:c.3567-11T>A	ENSP00000345629.4:n.3567-11T>A
ENST00000359173.7:c.2895-11T>A
ENST00000470101.1:n.985-11T>A
ENST00000518578.5:n.3629-11T>A
NM_001001671.3:c.3567-11T>A	NP_001001671.3:n.3567-11T>A
XM_011545507.1:c.3222-11T>A	XP_011543809.1:n.3222-11T>A
XM_011545508.1:c.3135-11T>A	XP_011543810.1:n.3135-11T>A
XM_011545509.1:c.2532-11T>A	XP_011543811.1:n.2532-11T>A
XM_011545510.1:c.2241-11T>A	XP_011543812.1:n.2241-11T>A
XM_011545511.1:c.1872-11T>A	XP_011543813.1:n.1872-11T>A
XM_011545507.3:c.3222-11T>A	XP_011543809.3:n.3222-11T>A
XM_011545508.3:c.3135-11T>A	XP_011543810.3:n.3135-11T>A
XM_011545510.2:c.2241-11T>A	XP_011543812.1:n.2241-11T>A
XM_011545511.2:c.1872-11T>A	XP_011543813.1:n.1872-11T>A
NM_001001671.4:c.3567-11T>A MANE Select	NP_001001671.3:n.3567-11T>A