Canonical Allele Identifier: CA706933456

Gene: SAMD4A

Linked Data

• dbSNP Id: rs1957358
• MyVariant Identifiers: chr14:g.55222475T>A (hg19) ; chr14:g.54755757T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54755757T>A , CM000676.2:g.54755757T>A	GRCh38
NC_000014.8:g.55222475T>A , CM000676.1:g.55222475T>A	GRCh37
NC_000014.7:g.54292225T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000554335.6:c.1176+4220T>A MANE Select	ENSP00000452535.1:n.1176+4220T>A
ENST00000251091.9:c.912+4220T>A	ENSP00000251091.5:n.912+4220T>A
ENST00000392067.7:c.1176+4220T>A	ENSP00000375919.3:n.1176+4220T>A
ENST00000554335.5:c.1176+4220T>A	ENSP00000452535.1:n.1176+4220T>A
ENST00000555192.1:c.-52+860T>A	ENSP00000450808.1:n.-52+860T>A
ENST00000631086.2:c.-52+4220T>A	ENSP00000486821.1:n.-52+4220T>A
NM_001161576.2:c.912+4220T>A	NP_001155048.2:n.912+4220T>A
NM_001161577.1:c.-52+860T>A	NP_001155049.1:n.-52+860T>A
NM_015589.5:c.1176+4220T>A	NP_056404.4:n.1176+4220T>A
XM_024449514.1:c.1176+4220T>A	XP_024305282.1:n.1176+4220T>A
XM_024449515.1:c.1176+4220T>A	XP_024305283.1:n.1176+4220T>A
XM_024449516.1:c.1176+4220T>A	XP_024305284.1:n.1176+4220T>A
XM_024449517.1:c.912+4220T>A	XP_024305285.1:n.912+4220T>A
XM_024449518.1:c.873+4220T>A	XP_024305286.1:n.873+4220T>A
XM_024449519.1:c.609+4220T>A	XP_024305287.1:n.609+4220T>A
NM_001161577.2:c.-52+860T>A	NP_001155049.1:n.-52+860T>A
NM_015589.6:c.1176+4220T>A MANE Select	NP_056404.4:n.1176+4220T>A