Canonical Allele Identifier: CA663406189

Gene: MKX

Linked Data

• dbSNP Id: rs1395295138
• gnomAD v3: 10-27736904-CA-C
• gnomAD v4: 10-27736904-CA-C
• MyVariant Identifiers: chr10:g.28025834del (hg19) ; chr10:g.27736905del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27736906del , CM000672.2:g.27736906del	GRCh38
NC_000010.10:g.28025835del , CM000672.1:g.28025835del	GRCh37
NC_000010.9:g.28065841del	NCBI36
NG_029181.1:g.13945del

Transcript Alleles

HGVS	Amino-acid change
ENST00000419761.6:c.349-1531del MANE Select	ENSP00000400896.1:n.349-1531del
ENST00000375790.9:c.349-1531del	ENSP00000364946.4:n.349-1531del
ENST00000419761.5:c.349-1531del	ENSP00000400896.1:n.349-1531del
ENST00000460919.2:c.349-1531del	ENSP00000452751.1:n.349-1531del
NM_001242702.1:c.349-1531del	NP_001229631.1:n.349-1531del
NM_173576.2:c.349-1531del	NP_775847.2:n.349-1531del
XM_006717438.2:c.349-1531del	XP_006717501.1:n.349-1531del
XM_006717440.2:c.349-1531del	XP_006717503.1:n.349-1531del
XM_011519450.1:c.349-1531del	XP_011517752.1:n.349-1531del
XM_017016105.1:c.349-1531del	XP_016871594.1:n.349-1531del
XM_017016106.1:c.349-1531del	XP_016871595.1:n.349-1531del
XM_017016107.1:c.349-1531del	XP_016871596.1:n.349-1531del
XM_017016108.1:c.349-1531del	XP_016871597.1:n.349-1531del
NM_173576.3:c.349-1531del MANE Select	NP_775847.2:n.349-1531del
NM_001242702.2:c.349-1531del	NP_001229631.1:n.349-1531del