Canonical Allele Identifier: CA401324407

Gene: CCDC40

Linked Data

• dbSNP Id: rs2037821598
• MyVariant Identifiers: chr17:g.78032663T>C (hg19) ; chr17:g.80058864T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80058864T>C , CM000679.2:g.80058864T>C	GRCh38
NC_000017.10:g.78032663T>C , CM000679.1:g.78032663T>C	GRCh37
NC_000017.9:g.75647258T>C	NCBI36
NG_029761.1:g.27233T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397545.9:c.1324T>C MANE Select	ENSP00000380679.4:p.Tyr442His
ENST00000269318.9:c.1324T>C	ENSP00000269318.5:p.Tyr442His
ENST00000374876.4:c.1317+213T>C	ENSP00000364010.4:n.1317+213T>C
ENST00000374877.7:c.1324T>C	ENSP00000364011.3:p.Tyr442His
ENST00000397545.8:c.1324T>C	ENSP00000380679.4:p.Tyr442His
ENST00000574799.5:n.861T>C
NM_001243342.1:c.1324T>C	NP_001230271.1:p.Tyr442His
NM_017950.3:c.1324T>C	NP_060420.2:p.Tyr442His
XM_005257492.3:c.1324T>C	XP_005257549.1:p.Tyr442His
XM_011524963.1:c.1234T>C	XP_011523265.1:p.Tyr412His
XM_011524964.1:c.145T>C	XP_011523266.1:p.Tyr49His
XM_011524965.1:c.1324T>C	XP_011523267.1:p.Tyr442His
XR_934495.1:n.1355T>C
NM_001330508.1:c.1324T>C	NP_001317437.1:p.Tyr442His
XM_011524963.3:c.1234T>C	XP_011523265.1:p.Tyr412His
XM_011524964.3:c.145T>C	XP_011523266.1:p.Tyr49His
XM_011524965.3:c.1324T>C	XP_011523267.1:p.Tyr442His
XM_017024807.1:c.1324T>C	XP_016880296.1:p.Tyr442His
XM_024450821.1:c.1234T>C	XP_024306589.1:p.Tyr412His
XR_001752550.2:n.1355T>C
XR_934495.2:n.1355T>C
NM_017950.4:c.1324T>C MANE Select	NP_060420.2:p.Tyr442His
NM_001330508.2:c.1324T>C	NP_001317437.1:p.Tyr442His
NM_001243342.2:c.1324T>C	NP_001230271.1:p.Tyr442His