Canonical Allele Identifier: CA1584849668

Gene: SMAD5

Linked Data

• dbSNP Id: rs1109158
• gnomAD v4: 5-136163522-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.136163522T>G , CM000667.2:g.136163522T>G	GRCh38
NC_000005.9:g.135499211T>G , CM000667.1:g.135499211T>G	GRCh37
NC_000005.8:g.135527110T>G	NCBI36
NG_032037.1:g.35676T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000509297.6:c.775+131T>G	ENSP00000426696.2:n.775+131T>G
ENST00000545279.6:c.775+131T>G MANE Select	ENSP00000441954.2:n.775+131T>G
ENST00000507637.1:c.242+131T>G
ENST00000514777.1:n.60-8912T>G
ENST00000545279.5:c.775+131T>G	ENSP00000441954.2:n.775+131T>G
ENST00000545620.5:c.775+131T>G	ENSP00000446474.2:n.775+131T>G
NM_001001419.2:c.775+131T>G	NP_001001419.1:n.775+131T>G
NM_001001420.2:c.775+131T>G	NP_001001420.1:n.775+131T>G
NM_005903.6:c.775+131T>G	NP_005894.3:n.775+131T>G
XM_017009470.2:c.775+131T>G	XP_016864959.1:n.775+131T>G
XM_024446046.1:c.775+131T>G	XP_024301814.1:n.775+131T>G
XM_024446047.1:c.775+131T>G	XP_024301815.1:n.775+131T>G
NM_005903.7:c.775+131T>G MANE Select	NP_005894.3:n.775+131T>G
NM_001001419.3:c.775+131T>G	NP_001001419.1:n.775+131T>G
NM_001001420.3:c.775+131T>G	NP_001001420.1:n.775+131T>G