Canonical Allele Identifier: CA357204656
Gene: GC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71756723T>G , CM000666.2:g.71756723T>G GRCh38
NC_000004.11:g.72622440T>G , CM000666.1:g.72622440T>G GRCh37
NC_000004.10:g.72841304T>G NCBI36
NG_012837.2:g.53798A>C
NG_012837.3:g.53798A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000273951.13:c.1023A>C MANE Select ENSP00000273951.8:p.Lys341Asn
ENST00000273951.12:c.1023A>C ENSP00000273951.8:p.Lys341Asn
ENST00000503472.5:n.907A>C
ENST00000504199.5:c.1080A>C ENSP00000421725.1:p.Lys360Asn
ENST00000509740.5:c.1023A>C ENSP00000422664.1:p.Lys341Asn
ENST00000513476.5:c.1023A>C ENSP00000426683.1:p.Lys341Asn
NM_000583.3:c.1023A>C NP_000574.2:p.Lys341Asn
NM_001204306.1:c.1023A>C NP_001191235.1:p.Lys341Asn
NM_001204307.1:c.1080A>C NP_001191236.1:p.Lys360Asn
XM_006714177.2:c.1023A>C XP_006714240.1:p.Lys341Asn
XM_006714177.3:c.1023A>C XP_006714240.1:p.Lys341Asn
NM_000583.4:c.1023A>C MANE Select NP_000574.2:p.Lys341Asn