Canonical Allele Identifier: CA432437769

Linked Data

MyVariant Identifiers: chr3:g.10331536T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10289852T>A , CM000665.2:g.10289852T>A GRCh38
NC_000003.11:g.10331536T>A , CM000665.1:g.10331536T>A GRCh37
NC_000003.10:g.10306536T>A NCBI36
NG_011560.1:g.8096A>T
NG_033090.1:g.13901T>A
NG_033090.2:g.13901T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000335542.13:c.135A>T (GHRL) MANE Select ENSP00000335074.8:p.Pro45=
ENST00000287656.11:c.132A>T (GHRL) ENSP00000287656.7:p.Pro44=
ENST00000335542.12:c.135A>T (GHRL) ENSP00000335074.8:p.Pro45=
ENST00000422159.5:c.135A>T (GHRL) ENSP00000405464.1:p.Pro45=
ENST00000429122.1:c.135A>T (GHRL) ENSP00000414819.1:p.Pro45=
ENST00000430179.5:c.132A>T (GHRL) ENSP00000399922.1:p.Pro44=
ENST00000437422.6:c.99A>T (GHRL) ENSP00000416768.2:p.Pro33=
ENST00000439975.6:c.72+2990A>T (GHRL) ENSP00000403725.2:n.72+2990A>T
ENST00000446937.2:c.72+2990A>T (GHRL) ENSP00000394923.2:n.72+2990A>T
ENST00000449238.6:c.96A>T (GHRL) ENSP00000388145.2:p.Pro32=
ENST00000457360.5:c.135A>T (GHRL) ENSP00000391406.1:p.Pro45=
ENST00000481287.5:n.312A>T (GHRL)
ENST00000491589.5:n.226A>T (GHRL)
NM_001134941.2:c.132A>T (GHRL) NP_001128413.1:p.Pro44=
NM_001134944.1:c.99A>T (GHRL) NP_001128416.1:p.Pro33=
NM_001134945.1:c.96A>T (GHRL) NP_001128417.1:p.Pro32=
NM_001134946.1:c.72+2990A>T (GHRL) NP_001128418.1:n.72+2990A>T
NM_001302821.1:c.135A>T (GHRL) NP_001289750.1:p.Pro45=
NM_001302822.1:c.135A>T (GHRL) NP_001289751.1:p.Pro45=
NM_001302823.1:c.132A>T (GHRL) NP_001289752.1:p.Pro44=
NM_001302824.1:c.135A>T (GHRL) NP_001289753.1:p.Pro45=
NM_001302825.1:c.135A>T (GHRL) NP_001289754.1:p.Pro45=
NM_016362.4:c.135A>T (GHRL) NP_057446.1:p.Pro45=
NR_004431.3:n.383+1750T>A (GHRLOS)
NR_024144.2:n.466+1750T>A (GHRLOS)
NR_024145.2:n.555+1750T>A (GHRLOS)
NR_073566.1:n.566+1746T>A (GHRLOS)
NR_073567.1:n.554+1750T>A (GHRLOS)
NR_073568.1:n.409+1750T>A (GHRLOS)
NR_126505.1:n.106+2990A>T (GHRL)
XM_017006612.2:c.135A>T (GHRL) XP_016862101.1:p.Pro45=
XM_017006613.2:c.132A>T (GHRL) XP_016862102.1:p.Pro44=
XM_024453594.1:c.135A>T (GHRL) XP_024309362.1:p.Pro45=
NM_001134941.3:c.132A>T (GHRL) NP_001128413.1:p.Pro44=
NM_001134944.2:c.99A>T (GHRL) NP_001128416.1:p.Pro33=
NM_001134945.2:c.96A>T (GHRL) NP_001128417.1:p.Pro32=
NM_001134946.2:c.72+2990A>T (GHRL) NP_001128418.1:n.72+2990A>T
NM_001302821.2:c.135A>T (GHRL) NP_001289750.1:p.Pro45=
NM_001302822.2:c.135A>T (GHRL) NP_001289751.1:p.Pro45=
NM_001302823.2:c.132A>T (GHRL) NP_001289752.1:p.Pro44=
NM_001302824.2:c.135A>T (GHRL) NP_001289753.1:p.Pro45=
NM_001302825.2:c.135A>T (GHRL) NP_001289754.1:p.Pro45=
NM_016362.5:c.135A>T (GHRL) MANE Select NP_057446.1:p.Pro45=
NR_126505.2:n.106+2990A>T (GHRL)