Canonical Allele Identifier: CA124994502

Gene: MCC

Linked Data

• dbSNP Id: rs143092740
• MyVariant Identifiers: chr5:g.112399691_112399692insG (hg19) ; chr5:g.113063994_113063995insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113063995dup , CM000667.2:g.113063995dup	GRCh38
NC_000005.9:g.112399692dup , CM000667.1:g.112399692dup	GRCh37
NC_000005.8:g.112427591dup	NCBI36
NG_012265.1:g.429836dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302475.9:c.1632dup	ENSP00000305617.4:p.Ser545GlnfsTer12
ENST00000408903.7:c.2202dup MANE Select	ENSP00000386227.3:p.Ser735GlnfsTer12
ENST00000302475.8:c.1632dup	ENSP00000305617.4:p.Ser545GlnfsTer12
ENST00000408903.6:c.2202dup	ENSP00000386227.3:p.Ser735GlnfsTer12
ENST00000514701.5:c.1632dup	ENSP00000485220.1:p.Ser545GlnfsTer12
ENST00000515367.6:c.1443dup	ENSP00000421615.2:p.Ser482GlnfsTer12
ENST00000624689.3:c.46dup
NM_001085377.1:c.2202dup	NP_001078846.1:p.Ser735GlnfsTer12
NM_002387.2:c.1632dup	NP_002378.1:p.Ser545GlnfsTer12
XM_005271991.2:c.1632dup	XP_005272048.1:p.Ser545GlnfsTer12
XM_005271991.3:c.1632dup	XP_005272048.1:p.Ser545GlnfsTer12
XM_017009473.1:c.2202dup	XP_016864962.1:p.Ser735GlnfsTer12
XM_017009474.1:c.1602dup	XP_016864963.1:p.Ser535GlnfsTer12
XM_024446049.1:c.1443dup	XP_024301817.1:p.Ser482GlnfsTer12
XM_024446050.1:c.1443dup	XP_024301818.1:p.Ser482GlnfsTer12
XM_024446051.1:c.1443dup	XP_024301819.1:p.Ser482GlnfsTer12
XM_024446052.1:c.1443dup	XP_024301820.1:p.Ser482GlnfsTer12
NM_001085377.2:c.2202dup MANE Select	NP_001078846.2:p.Ser735GlnfsTer12
NM_002387.3:c.1632dup	NP_002378.2:p.Ser545GlnfsTer12