Canonical Allele Identifier: CA2830535902

Gene: GOLIM4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.168025191G>A , CM000665.2:g.168025191G>A	GRCh38
NC_000003.11:g.167742979G>A , CM000665.1:g.167742979G>A	GRCh37
NC_000003.10:g.169225673G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470487.6:c.1624-96C>T MANE Select	ENSP00000417354.1:n.1624-96C>T
ENST00000309027.4:c.1540-96C>T	ENSP00000309893.4:n.1540-96C>T
ENST00000470487.5:c.1624-96C>T	ENSP00000417354.1:n.1624-96C>T
NM_001308155.1:c.1540-96C>T	NP_001295084.1:n.1540-96C>T
NM_014498.3:c.1624-96C>T	NP_055313.1:n.1624-96C>T
NM_014498.4:c.1624-96C>T	NP_055313.1:n.1624-96C>T
XM_005247364.1:c.1627-96C>T	XP_005247421.1:n.1627-96C>T
XM_005247365.1:c.1543-96C>T	XP_005247422.1:n.1543-96C>T
XM_005247364.3:c.1627-96C>T	XP_005247421.1:n.1627-96C>T
XM_005247365.3:c.1543-96C>T	XP_005247422.1:n.1543-96C>T
XM_017006183.1:c.1186-96C>T	XP_016861672.1:n.1186-96C>T
XM_024453455.1:c.1183-96C>T	XP_024309223.1:n.1183-96C>T
NM_001308155.2:c.1540-96C>T	NP_001295084.1:n.1540-96C>T
NM_014498.5:c.1624-96C>T MANE Select	NP_055313.1:n.1624-96C>T