Canonical Allele Identifier: CA12976252

Gene: GPSM1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136357696G>A , CM000671.2:g.136357696G>A	GRCh38
NC_000009.11:g.139252148G>A , CM000671.1:g.139252148G>A	GRCh37
NC_000009.10:g.138371969G>A	NCBI36
NG_028088.2:g.35153G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354753.7:c.1918-318G>A	ENSP00000346797.4:n.1918-318G>A
ENST00000440944.6:c.1822-318G>A MANE Select	ENSP00000392828.1:n.1822-318G>A
ENST00000291775.3:c.295-318G>A	ENSP00000291775.3:n.295-318G>A
ENST00000354753.6:c.1754-318G>A
ENST00000392944.5:c.295-318G>A	ENSP00000376673.1:n.295-318G>A
ENST00000429455.5:c.295-318G>A	ENSP00000390705.1:n.295-318G>A
ENST00000440944.5:c.1822-318G>A	ENSP00000392828.1:n.1822-318G>A
NM_001145638.2:c.1822-318G>A	NP_001139110.2:n.1822-318G>A
NM_001145639.1:c.295-318G>A	NP_001139111.1:n.295-318G>A
NM_001200003.1:c.295-318G>A	NP_001186932.1:n.295-318G>A
XM_011518498.1:c.1918-318G>A	XP_011516800.1:n.1918-318G>A
XM_011518498.2:c.1918-318G>A	XP_011516800.1:n.1918-318G>A
XM_017014598.2:c.1840-318G>A	XP_016870087.1:n.1840-318G>A
XM_017014599.2:c.295-318G>A	XP_016870088.1:n.295-318G>A
XM_024447499.1:c.295-318G>A	XP_024303267.1:n.295-318G>A
NM_001145638.3:c.1822-318G>A MANE Select	NP_001139110.2:n.1822-318G>A
NM_001200003.2:c.295-318G>A	NP_001186932.1:n.295-318G>A
NM_001145639.2:c.295-318G>A	NP_001139111.1:n.295-318G>A