Canonical Allele Identifier: CA445979284
Gene: MCC HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.112399719C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113064022C>G , CM000667.2:g.113064022C>G GRCh38
NC_000005.9:g.112399719C>G , CM000667.1:g.112399719C>G GRCh37
NC_000005.8:g.112427618C>G NCBI36
NG_012265.1:g.429809G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000302475.9:c.1605G>C ENSP00000305617.4:p.Val535=
ENST00000408903.7:c.2175G>C MANE Select ENSP00000386227.3:p.Val725=
ENST00000302475.8:c.1605G>C ENSP00000305617.4:p.Val535=
ENST00000408903.6:c.2175G>C ENSP00000386227.3:p.Val725=
ENST00000514701.5:c.1605G>C ENSP00000485220.1:p.Val535=
ENST00000515367.6:c.1416G>C ENSP00000421615.2:p.Val472=
ENST00000624689.3:c.19G>C
NM_001085377.1:c.2175G>C NP_001078846.1:p.Val725=
NM_002387.2:c.1605G>C NP_002378.1:p.Val535=
XM_005271991.2:c.1605G>C XP_005272048.1:p.Val535=
XM_005271991.3:c.1605G>C XP_005272048.1:p.Val535=
XM_017009473.1:c.2175G>C XP_016864962.1:p.Val725=
XM_017009474.1:c.1575G>C XP_016864963.1:p.Val525=
XM_024446049.1:c.1416G>C XP_024301817.1:p.Val472=
XM_024446050.1:c.1416G>C XP_024301818.1:p.Val472=
XM_024446051.1:c.1416G>C XP_024301819.1:p.Val472=
XM_024446052.1:c.1416G>C XP_024301820.1:p.Val472=
NM_001085377.2:c.2175G>C MANE Select NP_001078846.2:p.Val725=
NM_002387.3:c.1605G>C NP_002378.2:p.Val535=