Canonical Allele Identifier: CA445979278

Gene: MCC

Linked Data

• MyVariant Identifiers: chr5:g.112399713G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113064016G>C , CM000667.2:g.113064016G>C	GRCh38
NC_000005.9:g.112399713G>C , CM000667.1:g.112399713G>C	GRCh37
NC_000005.8:g.112427612G>C	NCBI36
NG_012265.1:g.429815C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302475.9:c.1611C>G	ENSP00000305617.4:p.Pro537=
ENST00000408903.7:c.2181C>G MANE Select	ENSP00000386227.3:p.Pro727=
ENST00000302475.8:c.1611C>G	ENSP00000305617.4:p.Pro537=
ENST00000408903.6:c.2181C>G	ENSP00000386227.3:p.Pro727=
ENST00000514701.5:c.1611C>G	ENSP00000485220.1:p.Pro537=
ENST00000515367.6:c.1422C>G	ENSP00000421615.2:p.Pro474=
ENST00000624689.3:c.25C>G
NM_001085377.1:c.2181C>G	NP_001078846.1:p.Pro727=
NM_002387.2:c.1611C>G	NP_002378.1:p.Pro537=
XM_005271991.2:c.1611C>G	XP_005272048.1:p.Pro537=
XM_005271991.3:c.1611C>G	XP_005272048.1:p.Pro537=
XM_017009473.1:c.2181C>G	XP_016864962.1:p.Pro727=
XM_017009474.1:c.1581C>G	XP_016864963.1:p.Pro527=
XM_024446049.1:c.1422C>G	XP_024301817.1:p.Pro474=
XM_024446050.1:c.1422C>G	XP_024301818.1:p.Pro474=
XM_024446051.1:c.1422C>G	XP_024301819.1:p.Pro474=
XM_024446052.1:c.1422C>G	XP_024301820.1:p.Pro474=
NM_001085377.2:c.2181C>G MANE Select	NP_001078846.2:p.Pro727=
NM_002387.3:c.1611C>G	NP_002378.2:p.Pro537=