Canonical Allele Identifier: CA2261795608

Gene: MAP3K14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45306118G= , CM000679.2:g.45306118G=	GRCh38
NC_000017.10:g.43383484G= , CM000679.1:g.43383484G=	GRCh37
NC_000017.9:g.40739267G=	NCBI36
NG_033823.1:g.15931C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003954.5:c.-21+10842C= MANE Select	NP_003945.2:n.-21+10842C=
ENST00000344686.8:c.-21+10842C= MANE Select	ENSP00000478552.1:n.-21+10842C=
NM_003954.4:c.-21+10842C=	NP_003945.2:n.-21+10842C=
ENST00000344686.6:c.-21+10842C=	ENSP00000478552.1:n.-21+10842C=
ENST00000617331.1:c.-21+10842C=	ENSP00000480974.1:n.-21+10842C=
ENST00000617331.3:c.-21+6167C=	ENSP00000480974.3:n.-21+6167C=
XM_011525441.1:c.-21+6167C=	XP_011523743.1:n.-21+6167C=
XM_011525441.2:c.-21+6167C=	XP_011523743.1:n.-21+6167C=
XR_934591.1:n.89+10842C=