Canonical Allele Identifier: CA467223857

Gene: SH2D3C

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127741791G>C , CM000671.2:g.127741791G>C	GRCh38
NC_000009.11:g.130504070G>C , CM000671.1:g.130504070G>C	GRCh37
NC_000009.10:g.129543891G>C	NCBI36
NG_030563.1:g.41979C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314830.13:c.2085C>G MANE Select	ENSP00000317817.8:p.Ala695=
ENST00000314830.12:c.2085C>G	ENSP00000317817.8:p.Ala695=
ENST00000373276.7:c.1881C>G	ENSP00000362373.3:p.Ala627=
ENST00000373277.8:c.1614C>G	ENSP00000362374.4:p.Ala538=
ENST00000420366.5:c.1611C>G	ENSP00000388536.1:p.Ala537=
ENST00000429553.5:c.1023C>G	ENSP00000394632.1:p.Ala341=
ENST00000629203.2:c.1605C>G	ENSP00000485866.1:p.Ala535=
NM_001142531.1:c.1023C>G	NP_001136003.1:p.Ala341=
NM_001142532.1:c.1023C>G	NP_001136004.1:p.Ala341=
NM_001142533.1:c.1611C>G	NP_001136005.1:p.Ala537=
NM_001142534.1:c.1605C>G	NP_001136006.1:p.Ala535=
NM_001252334.1:c.1881C>G	NP_001239263.1:p.Ala627=
NM_005489.3:c.1614C>G	NP_005480.2:p.Ala538=
NM_170600.2:c.2085C>G	NP_733745.1:p.Ala695=
XM_005251639.1:c.1023C>G	XP_005251696.1:p.Ala341=
XM_011518114.1:c.1917C>G	XP_011516416.1:p.Ala639=
XM_011518115.1:c.1917C>G	XP_011516417.1:p.Ala639=
XM_011518116.1:c.1917C>G	XP_011516418.1:p.Ala639=
XM_011518117.1:c.1023C>G	XP_011516419.1:p.Ala341=
XM_011518114.2:c.1917C>G	XP_011516416.1:p.Ala639=
XM_011518115.2:c.1917C>G	XP_011516417.1:p.Ala639=
XM_011518117.3:c.1023C>G	XP_011516419.1:p.Ala341=
NM_170600.3:c.2085C>G MANE Select	NP_733745.1:p.Ala695=
NM_005489.4:c.1614C>G	NP_005480.2:p.Ala538=
NM_001252334.2:c.1881C>G	NP_001239263.1:p.Ala627=