Canonical Allele Identifier: CA711927172

Gene: GOLGA8H DNM1P50 ARHGAP11B-DT

Linked Data

• dbSNP Id: rs1375691274
• gnomAD v3: 15-30606372-A-G
• gnomAD v4: 15-30606372-A-G
• MyVariant Identifiers: chr15:g.30898575A>G (hg19) ; chr15:g.30606372A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.30606372A>G , CM000677.2:g.30606372A>G	GRCh38
NC_000015.9:g.30898575A>G , CM000677.1:g.30898575A>G	GRCh37
NC_000015.8:g.28685867A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000566740.2:c.168+410A>G (GOLGA8H) MANE Select	ENSP00000456894.1:n.168+410A>G
ENST00000566740.1:c.168+410A>G (GOLGA8H)	ENSP00000456894.1:n.168+410A>G
NM_001282490.1:c.168+410A>G (GOLGA8H)	NP_001269419.1:n.168+410A>G
XM_006720672.2:c.129+410A>G (GOLGA8H)	XP_006720735.1:n.129+410A>G
XM_011521990.1:c.-286+410A>G (GOLGA8H)	XP_011520292.1:n.-286+410A>G
XM_011522274.1:c.-308+1846T>C (DNM1P50)	XP_011520576.1:n.-308+1846T>C
XM_011522275.1:c.-308+1846T>C (DNM1P50)	XP_011520577.1:n.-308+1846T>C
XM_011522276.1:c.-308+1846T>C (DNM1P50)	XP_011520578.1:n.-308+1846T>C
XM_011522278.1:c.-308+1846T>C (DNM1P50)	XP_011520580.1:n.-308+1846T>C
XM_011522282.1:c.209+1846T>C (DNM1P50)	XP_011520584.1:n.209+1846T>C
XM_011522283.1:c.209+1846T>C (DNM1P50)	XP_011520585.1:n.209+1846T>C
XR_932037.1:n.1044+1846T>C (DNM1P50)
XR_932039.1:n.1166+1846T>C (DNM1P50)
XR_932042.1:n.786+1846T>C (DNM1P50)
XR_932043.1:n.707+18679T>C (DNM1P50)
XR_932044.1:n.708-12080T>C (DNM1P50)
XR_932045.1:n.707+18679T>C (DNM1P50)
NR_157593.1:n.851-12080T>C (ARHGAP11B-DT)
NR_157594.1:n.849+1846T>C (ARHGAP11B-DT)
NR_157595.1:n.513-12080T>C (ARHGAP11B-DT)
NM_001282490.2:c.168+410A>G (GOLGA8H) MANE Select	NP_001269419.1:n.168+410A>G