Canonical Allele Identifier: CA1131436220

Gene: MAP3K15

Linked Data

• dbSNP Id: rs2147199459
• gnomAD v3: X-19362901-C-A
• gnomAD v4: X-19362901-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19362901C>A , CM000685.2:g.19362901C>A	GRCh38
NC_000023.10:g.19381019C>A , CM000685.1:g.19381019C>A	GRCh37
NC_000023.9:g.19290940C>A	NCBI36
NG_016781.1:g.24009C>A
NG_021184.1:g.157361G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338883.9:c.3567-51G>T MANE Select	ENSP00000345629.4:n.3567-51G>T
ENST00000338883.8:c.3567-51G>T	ENSP00000345629.4:n.3567-51G>T
ENST00000359173.7:c.2895-51G>T
ENST00000470101.1:n.985-51G>T
ENST00000518578.5:n.3629-51G>T
NM_001001671.3:c.3567-51G>T	NP_001001671.3:n.3567-51G>T
XM_011545507.1:c.3222-51G>T	XP_011543809.1:n.3222-51G>T
XM_011545508.1:c.3135-51G>T	XP_011543810.1:n.3135-51G>T
XM_011545509.1:c.2532-51G>T	XP_011543811.1:n.2532-51G>T
XM_011545510.1:c.2241-51G>T	XP_011543812.1:n.2241-51G>T
XM_011545511.1:c.1872-51G>T	XP_011543813.1:n.1872-51G>T
XM_011545507.3:c.3222-51G>T	XP_011543809.3:n.3222-51G>T
XM_011545508.3:c.3135-51G>T	XP_011543810.3:n.3135-51G>T
XM_011545510.2:c.2241-51G>T	XP_011543812.1:n.2241-51G>T
XM_011545511.2:c.1872-51G>T	XP_011543813.1:n.1872-51G>T
NM_001001671.4:c.3567-51G>T MANE Select	NP_001001671.3:n.3567-51G>T