Canonical Allele Identifier: CA432437719

Linked Data

gnomAD v4: 3-10289786-C-G
MyVariant Identifiers: chr3:g.10331470C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10289786C>G , CM000665.2:g.10289786C>G GRCh38
NC_000003.11:g.10331470C>G , CM000665.1:g.10331470C>G GRCh37
NC_000003.10:g.10306470C>G NCBI36
NG_011560.1:g.8162G>C
NG_033090.1:g.13835C>G
NG_033090.2:g.13835C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000335542.13:c.201G>C (GHRL) MANE Select ENSP00000335074.8:p.Gly67=
ENST00000287656.11:c.198G>C (GHRL) ENSP00000287656.7:p.Gly66=
ENST00000335542.12:c.201G>C (GHRL) ENSP00000335074.8:p.Gly67=
ENST00000422159.5:c.201G>C (GHRL) ENSP00000405464.1:p.Gly67=
ENST00000429122.1:c.201G>C (GHRL) ENSP00000414819.1:p.Gly67=
ENST00000430179.5:c.198G>C (GHRL) ENSP00000399922.1:p.Gly66=
ENST00000437422.6:c.165G>C (GHRL) ENSP00000416768.2:p.Gly55=
ENST00000439975.6:c.73-2974G>C (GHRL) ENSP00000403725.2:n.73-2974G>C
ENST00000446937.2:c.72+3056G>C (GHRL) ENSP00000394923.2:n.72+3056G>C
ENST00000449238.6:c.162G>C (GHRL) ENSP00000388145.2:p.Gly54=
ENST00000457360.5:c.201G>C (GHRL) ENSP00000391406.1:p.Gly67=
ENST00000475759.5:n.22G>C (GHRL)
ENST00000476283.1:n.22G>C (GHRL)
ENST00000481287.5:n.378G>C (GHRL)
ENST00000491589.5:n.292G>C (GHRL)
NM_001134941.2:c.198G>C (GHRL) NP_001128413.1:p.Gly66=
NM_001134944.1:c.165G>C (GHRL) NP_001128416.1:p.Gly55=
NM_001134945.1:c.162G>C (GHRL) NP_001128417.1:p.Gly54=
NM_001134946.1:c.73-2974G>C (GHRL) NP_001128418.1:n.73-2974G>C
NM_001302821.1:c.201G>C (GHRL) NP_001289750.1:p.Gly67=
NM_001302822.1:c.201G>C (GHRL) NP_001289751.1:p.Gly67=
NM_001302823.1:c.198G>C (GHRL) NP_001289752.1:p.Gly66=
NM_001302824.1:c.201G>C (GHRL) NP_001289753.1:p.Gly67=
NM_001302825.1:c.201G>C (GHRL) NP_001289754.1:p.Gly67=
NM_016362.4:c.201G>C (GHRL) NP_057446.1:p.Gly67=
NR_004431.3:n.383+1684C>G (GHRLOS)
NR_024144.2:n.466+1684C>G (GHRLOS)
NR_024145.2:n.555+1684C>G (GHRLOS)
NR_073566.1:n.566+1680C>G (GHRLOS)
NR_073567.1:n.554+1684C>G (GHRLOS)
NR_073568.1:n.409+1684C>G (GHRLOS)
NR_126505.1:n.106+3056G>C (GHRL)
XM_017006612.2:c.201G>C (GHRL) XP_016862101.1:p.Gly67=
XM_017006613.2:c.198G>C (GHRL) XP_016862102.1:p.Gly66=
XM_024453594.1:c.201G>C (GHRL) XP_024309362.1:p.Gly67=
NM_001134941.3:c.198G>C (GHRL) NP_001128413.1:p.Gly66=
NM_001134944.2:c.165G>C (GHRL) NP_001128416.1:p.Gly55=
NM_001134945.2:c.162G>C (GHRL) NP_001128417.1:p.Gly54=
NM_001134946.2:c.73-2974G>C (GHRL) NP_001128418.1:n.73-2974G>C
NM_001302821.2:c.201G>C (GHRL) NP_001289750.1:p.Gly67=
NM_001302822.2:c.201G>C (GHRL) NP_001289751.1:p.Gly67=
NM_001302823.2:c.198G>C (GHRL) NP_001289752.1:p.Gly66=
NM_001302824.2:c.201G>C (GHRL) NP_001289753.1:p.Gly67=
NM_001302825.2:c.201G>C (GHRL) NP_001289754.1:p.Gly67=
NM_016362.5:c.201G>C (GHRL) MANE Select NP_057446.1:p.Gly67=
NR_126505.2:n.106+3056G>C (GHRL)