Canonical Allele Identifier: CA3370013

Gene: MCC

Linked Data

• dbSNP Id: rs377672005
• ExAC: 5:112399739 C / T
• MyVariant Identifiers: chr5:g.112399739C>T (hg19) ; chr5:g.113064042C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113064042C>T , CM000667.2:g.113064042C>T	GRCh38
NC_000005.9:g.112399739C>T , CM000667.1:g.112399739C>T	GRCh37
NC_000005.8:g.112427638C>T	NCBI36
NG_012265.1:g.429789G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302475.9:c.1585G>A	ENSP00000305617.4:p.Ala529Thr
ENST00000408903.7:c.2155G>A MANE Select	ENSP00000386227.3:p.Ala719Thr
ENST00000302475.8:c.1585G>A	ENSP00000305617.4:p.Ala529Thr
ENST00000408903.6:c.2155G>A	ENSP00000386227.3:p.Ala719Thr
ENST00000514701.5:c.1585G>A	ENSP00000485220.1:p.Ala529Thr
ENST00000515367.6:c.1396G>A	ENSP00000421615.2:p.Ala466Thr
NM_001085377.1:c.2155G>A	NP_001078846.1:p.Ala719Thr
NM_002387.2:c.1585G>A	NP_002378.1:p.Ala529Thr
XM_005271991.2:c.1585G>A	XP_005272048.1:p.Ala529Thr
XM_005271991.3:c.1585G>A	XP_005272048.1:p.Ala529Thr
XM_017009473.1:c.2155G>A	XP_016864962.1:p.Ala719Thr
XM_017009474.1:c.1555G>A	XP_016864963.1:p.Ala519Thr
XM_024446049.1:c.1396G>A	XP_024301817.1:p.Ala466Thr
XM_024446050.1:c.1396G>A	XP_024301818.1:p.Ala466Thr
XM_024446051.1:c.1396G>A	XP_024301819.1:p.Ala466Thr
XM_024446052.1:c.1396G>A	XP_024301820.1:p.Ala466Thr
NM_001085377.2:c.2155G>A MANE Select	NP_001078846.2:p.Ala719Thr
NM_002387.3:c.1585G>A	NP_002378.2:p.Ala529Thr