Canonical Allele Identifier: CA626317594

Gene: MAP3K14

Linked Data

• dbSNP Id: rs1409841972
• gnomAD v2: 17-43383488-AT-A
• gnomAD v3: 17-45306122-AT-A
• gnomAD v4: 17-45306122-AT-A
• MyVariant Identifiers: chr17:g.43383489del (hg19) ; chr17:g.45306123del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45306129del , CM000679.2:g.45306129del	GRCh38
NC_000017.10:g.43383495del , CM000679.1:g.43383495del	GRCh37
NC_000017.9:g.40739278del	NCBI36
NG_033823.1:g.15926del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344686.8:c.-21+10837del MANE Select	ENSP00000478552.1:n.-21+10837del
ENST00000617331.3:c.-21+6162del	ENSP00000480974.3:n.-21+6162del
ENST00000344686.6:c.-21+10837del	ENSP00000478552.1:n.-21+10837del
ENST00000617331.1:c.-21+10837del	ENSP00000480974.1:n.-21+10837del
NM_003954.4:c.-21+10837del	NP_003945.2:n.-21+10837del
XM_011525441.1:c.-21+6162del	XP_011523743.1:n.-21+6162del
XR_934591.1:n.89+10837del
NM_003954.5:c.-21+10837del MANE Select	NP_003945.2:n.-21+10837del
XM_011525441.2:c.-21+6162del	XP_011523743.1:n.-21+6162del