Canonical Allele Identifier: CA360626270

Gene: MCC

Linked Data

• MyVariant Identifiers: chr5:g.112399810C>G (hg19) ; chr5:g.113064113C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113064113C>G , CM000667.2:g.113064113C>G	GRCh38
NC_000005.9:g.112399810C>G , CM000667.1:g.112399810C>G	GRCh37
NC_000005.8:g.112427709C>G	NCBI36
NG_012265.1:g.429718G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302475.9:c.1514G>C	ENSP00000305617.4:p.Cys505Ser
ENST00000408903.7:c.2084G>C MANE Select	ENSP00000386227.3:p.Cys695Ser
ENST00000302475.8:c.1514G>C	ENSP00000305617.4:p.Cys505Ser
ENST00000408903.6:c.2084G>C	ENSP00000386227.3:p.Cys695Ser
ENST00000514701.5:c.1514G>C	ENSP00000485220.1:p.Cys505Ser
ENST00000515367.6:c.1325G>C	ENSP00000421615.2:p.Cys442Ser
NM_001085377.1:c.2084G>C	NP_001078846.1:p.Cys695Ser
NM_002387.2:c.1514G>C	NP_002378.1:p.Cys505Ser
XM_005271991.2:c.1514G>C	XP_005272048.1:p.Cys505Ser
XM_005271991.3:c.1514G>C	XP_005272048.1:p.Cys505Ser
XM_017009473.1:c.2084G>C	XP_016864962.1:p.Cys695Ser
XM_017009474.1:c.1484G>C	XP_016864963.1:p.Cys495Ser
XM_024446049.1:c.1325G>C	XP_024301817.1:p.Cys442Ser
XM_024446050.1:c.1325G>C	XP_024301818.1:p.Cys442Ser
XM_024446051.1:c.1325G>C	XP_024301819.1:p.Cys442Ser
XM_024446052.1:c.1325G>C	XP_024301820.1:p.Cys442Ser
NM_001085377.2:c.2084G>C MANE Select	NP_001078846.2:p.Cys695Ser
NM_002387.3:c.1514G>C	NP_002378.2:p.Cys505Ser