Canonical Allele Identifier: CA772381192

Gene: MAP3K14

Linked Data

• dbSNP Id: rs1329640964
• gnomAD v3: 17-45306100-C-T
• gnomAD v4: 17-45306100-C-T
• MyVariant Identifiers: chr17:g.43383466C>T (hg19) ; chr17:g.45306100C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45306100C>T , CM000679.2:g.45306100C>T	GRCh38
NC_000017.10:g.43383466C>T , CM000679.1:g.43383466C>T	GRCh37
NC_000017.9:g.40739249C>T	NCBI36
NG_033823.1:g.15949G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344686.8:c.-21+10860G>A MANE Select	ENSP00000478552.1:n.-21+10860G>A
ENST00000617331.3:c.-21+6185G>A	ENSP00000480974.3:n.-21+6185G>A
ENST00000344686.6:c.-21+10860G>A	ENSP00000478552.1:n.-21+10860G>A
ENST00000617331.1:c.-21+10860G>A	ENSP00000480974.1:n.-21+10860G>A
NM_003954.4:c.-21+10860G>A	NP_003945.2:n.-21+10860G>A
XM_011525441.1:c.-21+6185G>A	XP_011523743.1:n.-21+6185G>A
XR_934591.1:n.89+10860G>A
NM_003954.5:c.-21+10860G>A MANE Select	NP_003945.2:n.-21+10860G>A
XM_011525441.2:c.-21+6185G>A	XP_011523743.1:n.-21+6185G>A