Canonical Allele Identifier: CA3370032

Gene: MCC

Linked Data

• dbSNP Id: rs767375752
• ExAC: 5:112399819 G / A
• gnomAD v2: 5-112399819-G-A
• gnomAD v4: 5-113064122-G-A
• MyVariant Identifiers: chr5:g.112399819G>A (hg19) ; chr5:g.113064122G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113064122G>A , CM000667.2:g.113064122G>A	GRCh38
NC_000005.9:g.112399819G>A , CM000667.1:g.112399819G>A	GRCh37
NC_000005.8:g.112427718G>A	NCBI36
NG_012265.1:g.429709C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302475.9:c.1505C>T	ENSP00000305617.4:p.Ala502Val
ENST00000408903.7:c.2075C>T MANE Select	ENSP00000386227.3:p.Ala692Val
ENST00000302475.8:c.1505C>T	ENSP00000305617.4:p.Ala502Val
ENST00000408903.6:c.2075C>T	ENSP00000386227.3:p.Ala692Val
ENST00000514701.5:c.1505C>T	ENSP00000485220.1:p.Ala502Val
ENST00000515367.6:c.1316C>T	ENSP00000421615.2:p.Ala439Val
NM_001085377.1:c.2075C>T	NP_001078846.1:p.Ala692Val
NM_002387.2:c.1505C>T	NP_002378.1:p.Ala502Val
XM_005271991.2:c.1505C>T	XP_005272048.1:p.Ala502Val
XM_005271991.3:c.1505C>T	XP_005272048.1:p.Ala502Val
XM_017009473.1:c.2075C>T	XP_016864962.1:p.Ala692Val
XM_017009474.1:c.1475C>T	XP_016864963.1:p.Ala492Val
XM_024446049.1:c.1316C>T	XP_024301817.1:p.Ala439Val
XM_024446050.1:c.1316C>T	XP_024301818.1:p.Ala439Val
XM_024446051.1:c.1316C>T	XP_024301819.1:p.Ala439Val
XM_024446052.1:c.1316C>T	XP_024301820.1:p.Ala439Val
NM_001085377.2:c.2075C>T MANE Select	NP_001078846.2:p.Ala692Val
NM_002387.3:c.1505C>T	NP_002378.2:p.Ala502Val