Canonical Allele Identifier: CA2830535900
Gene: GOLIM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.168025179_168025180insCCTTTT , CM000665.2:g.168025179_168025180insCCTTTT GRCh38
NC_000003.11:g.167742967_167742968insCCTTTT , CM000665.1:g.167742967_167742968insCCTTTT GRCh37
NC_000003.10:g.169225661_169225662insCCTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000470487.6:c.1624-85_1624-84insAAAAGG MANE Select ENSP00000417354.1:n.1624-85_1624-84insAAAAGG
ENST00000309027.4:c.1540-85_1540-84insAAAAGG ENSP00000309893.4:n.1540-85_1540-84insAAAAGG
ENST00000470487.5:c.1624-85_1624-84insAAAAGG ENSP00000417354.1:n.1624-85_1624-84insAAAAGG
NM_001308155.1:c.1540-85_1540-84insAAAAGG NP_001295084.1:n.1540-85_1540-84insAAAAGG
NM_014498.3:c.1624-85_1624-84insAAAAGG NP_055313.1:n.1624-85_1624-84insAAAAGG
NM_014498.4:c.1624-85_1624-84insAAAAGG NP_055313.1:n.1624-85_1624-84insAAAAGG
XM_005247364.1:c.1627-85_1627-84insAAAAGG XP_005247421.1:n.1627-85_1627-84insAAAAGG
XM_005247365.1:c.1543-85_1543-84insAAAAGG XP_005247422.1:n.1543-85_1543-84insAAAAGG
XM_005247364.3:c.1627-85_1627-84insAAAAGG XP_005247421.1:n.1627-85_1627-84insAAAAGG
XM_005247365.3:c.1543-85_1543-84insAAAAGG XP_005247422.1:n.1543-85_1543-84insAAAAGG
XM_017006183.1:c.1186-85_1186-84insAAAAGG XP_016861672.1:n.1186-85_1186-84insAAAAGG
XM_024453455.1:c.1183-85_1183-84insAAAAGG XP_024309223.1:n.1183-85_1183-84insAAAAGG
NM_001308155.2:c.1540-85_1540-84insAAAAGG NP_001295084.1:n.1540-85_1540-84insAAAAGG
NM_014498.5:c.1624-85_1624-84insAAAAGG MANE Select NP_055313.1:n.1624-85_1624-84insAAAAGG