Canonical Allele Identifier: CA2955574

Gene: GC

Linked Data

• dbSNP Id: rs755714409
• ExAC: 4:72622678 CTAAT / C
• gnomAD v2: 4-72622678-CTAAT-C
• gnomAD v4: 4-71756961-CTAAT-C
• MyVariant Identifiers: chr4:g.72622679_72622682del (hg19) ; chr4:g.71756962_71756965del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756965_71756968del , CM000666.2:g.71756965_71756968del	GRCh38
NC_000004.11:g.72622682_72622685del , CM000666.1:g.72622682_72622685del	GRCh37
NC_000004.10:g.72841546_72841549del	NCBI36
NG_012837.2:g.53556_53559del
NG_012837.3:g.53556_53559del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.832-51_832-48del MANE Select	ENSP00000273951.8:n.832-51_832-48del
ENST00000273951.12:c.832-51_832-48del	ENSP00000273951.8:n.832-51_832-48del
ENST00000503472.5:n.716-51_716-48del
ENST00000504199.5:c.889-51_889-48del	ENSP00000421725.1:n.889-51_889-48del
ENST00000509740.5:c.832-51_832-48del	ENSP00000422664.1:n.832-51_832-48del
ENST00000513476.5:c.832-51_832-48del	ENSP00000426683.1:n.832-51_832-48del
NM_000583.3:c.832-51_832-48del	NP_000574.2:n.832-51_832-48del
NM_001204306.1:c.832-51_832-48del	NP_001191235.1:n.832-51_832-48del
NM_001204307.1:c.889-51_889-48del	NP_001191236.1:n.889-51_889-48del
XM_006714177.2:c.832-51_832-48del	XP_006714240.1:n.832-51_832-48del
XM_006714177.3:c.832-51_832-48del	XP_006714240.1:n.832-51_832-48del
NM_000583.4:c.832-51_832-48del MANE Select	NP_000574.2:n.832-51_832-48del