Canonical Allele Identifier: CA515486809

Gene: MAP3K15

Linked Data

• MyVariant Identifiers: chrX:g.19380923A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19362805A>T , CM000685.2:g.19362805A>T	GRCh38
NC_000023.10:g.19380923A>T , CM000685.1:g.19380923A>T	GRCh37
NC_000023.9:g.19290844A>T	NCBI36
NG_016781.1:g.23913A>T
NG_021184.1:g.157457T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338883.9:c.3612T>A MANE Select	ENSP00000345629.4:p.Leu1204=
ENST00000338883.8:c.3612T>A	ENSP00000345629.4:p.Leu1204=
ENST00000359173.7:c.2940T>A
ENST00000470101.1:n.1030T>A
ENST00000518578.5:n.3674T>A
NM_001001671.3:c.3612T>A	NP_001001671.3:p.Leu1204=
XM_011545507.1:c.3267T>A	XP_011543809.1:p.Leu1089=
XM_011545508.1:c.3180T>A	XP_011543810.1:p.Leu1060=
XM_011545509.1:c.2577T>A	XP_011543811.1:p.Leu859=
XM_011545510.1:c.2286T>A	XP_011543812.1:p.Leu762=
XM_011545511.1:c.1917T>A	XP_011543813.1:p.Leu639=
XM_011545507.3:c.3267T>A	XP_011543809.3:p.Leu1089=
XM_011545508.3:c.3180T>A	XP_011543810.3:p.Leu1060=
XM_011545510.2:c.2286T>A	XP_011543812.1:p.Leu762=
XM_011545511.2:c.1917T>A	XP_011543813.1:p.Leu639=
NM_001001671.4:c.3612T>A MANE Select	NP_001001671.3:p.Leu1204=