Canonical Allele Identifier: CA2418227149

Gene: MAP3K15

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19362851C= , CM000685.2:g.19362851C=	GRCh38
NC_000023.10:g.19380969C= , CM000685.1:g.19380969C=	GRCh37
NC_000023.9:g.19290890C=	NCBI36
NG_016781.1:g.23959C=
NG_021184.1:g.157411G=

Transcript Alleles

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