Canonical Allele Identifier: CA824612902

Gene: DAAM2

Linked Data

• dbSNP Id: rs1460793391
• MyVariant Identifiers: chr6:g.39784384A>T (hg19) ; chr6:g.39816608A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39816608A>T , CM000668.2:g.39816608A>T	GRCh38
NC_000006.11:g.39784384A>T , CM000668.1:g.39784384A>T	GRCh37
NC_000006.10:g.39892362A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000274867.9:c.-57+24143A>T MANE Select	ENSP00000274867.4:n.-57+24143A>T
ENST00000274867.8:c.-57+24143A>T	ENSP00000274867.4:n.-57+24143A>T
ENST00000398904.6:c.-57+23465A>T	ENSP00000381876.2:n.-57+23465A>T
ENST00000475489.5:n.70+24143A>T
ENST00000491083.2:n.90+24143A>T
ENST00000494405.2:c.-57+24143A>T	ENSP00000488196.1:n.-57+24143A>T
ENST00000538976.5:c.-57+23465A>T	ENSP00000437808.1:n.-57+23465A>T
ENST00000633794.1:c.-57+24143A>T	ENSP00000488831.1:n.-57+24143A>T
NM_001201427.1:c.-57+24143A>T	NP_001188356.1:n.-57+24143A>T
NM_015345.3:c.-57+23465A>T	NP_056160.2:n.-57+23465A>T
XM_006715043.1:c.-57+24143A>T	XP_006715106.1:n.-57+24143A>T
XM_006715046.2:c.-57+23465A>T	XP_006715109.1:n.-57+23465A>T
XR_926775.1:n.38+3089T>A
XM_006715043.2:c.-57+24143A>T	XP_006715106.1:n.-57+24143A>T
XM_006715046.4:c.-57+23465A>T	XP_006715109.1:n.-57+23465A>T
XM_017010630.1:c.13+21857A>T	XP_016866119.1:n.13+21857A>T
NM_001201427.2:c.-57+24143A>T MANE Select	NP_001188356.1:n.-57+24143A>T
NM_015345.4:c.-57+23465A>T	NP_056160.2:n.-57+23465A>T