Canonical Allele Identifier: CA515486824

Gene: MAP3K15

Linked Data

• MyVariant Identifiers: chrX:g.19380953T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19362835T>G , CM000685.2:g.19362835T>G	GRCh38
NC_000023.10:g.19380953T>G , CM000685.1:g.19380953T>G	GRCh37
NC_000023.9:g.19290874T>G	NCBI36
NG_016781.1:g.23943T>G
NG_021184.1:g.157427A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338883.9:c.3582A>C MANE Select	ENSP00000345629.4:p.Leu1194=
ENST00000338883.8:c.3582A>C	ENSP00000345629.4:p.Leu1194=
ENST00000359173.7:c.2910A>C
ENST00000470101.1:n.1000A>C
ENST00000518578.5:n.3644A>C
NM_001001671.3:c.3582A>C	NP_001001671.3:p.Leu1194=
XM_011545507.1:c.3237A>C	XP_011543809.1:p.Leu1079=
XM_011545508.1:c.3150A>C	XP_011543810.1:p.Leu1050=
XM_011545509.1:c.2547A>C	XP_011543811.1:p.Leu849=
XM_011545510.1:c.2256A>C	XP_011543812.1:p.Leu752=
XM_011545511.1:c.1887A>C	XP_011543813.1:p.Leu629=
XM_011545507.3:c.3237A>C	XP_011543809.3:p.Leu1079=
XM_011545508.3:c.3150A>C	XP_011543810.3:p.Leu1050=
XM_011545510.2:c.2256A>C	XP_011543812.1:p.Leu752=
XM_011545511.2:c.1887A>C	XP_011543813.1:p.Leu629=
NM_001001671.4:c.3582A>C MANE Select	NP_001001671.3:p.Leu1194=