Canonical Allele Identifier: CA360011060

Gene: MCCC2

Linked Data

• MyVariant Identifiers: chr5:g.70898452T>A (hg19) ; chr5:g.71602625T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71602625T>A , CM000667.2:g.71602625T>A	GRCh38
NC_000005.9:g.70898452T>A , CM000667.1:g.70898452T>A	GRCh37
NC_000005.8:g.70934208T>A	NCBI36
NG_008882.1:g.20338T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.573T>A
ENST00000505787.8:n.2343T>A
ENST00000509358.7:c.503T>A	ENSP00000420994.3:p.Ile168Asn
ENST00000510895.7:n.626T>A
ENST00000629193.3:c.503T>A	ENSP00000486535.2:p.Ile168Asn
ENST00000681968.1:c.110T>A	ENSP00000508143.1:p.Ile37Asn
ENST00000682045.1:c.359T>A	ENSP00000507329.1:p.Ile120Asn
ENST00000682214.1:c.110T>A	ENSP00000507336.1:p.Ile37Asn
ENST00000682499.1:n.1324T>A
ENST00000682541.1:c.503T>A	ENSP00000507673.1:p.Ile168Asn
ENST00000682687.1:c.503T>A	ENSP00000507945.1:p.Ile168Asn
ENST00000682727.1:c.503T>A	ENSP00000507393.1:p.Ile168Asn
ENST00000682876.1:c.503T>A	ENSP00000508389.1:p.Ile168Asn
ENST00000683098.1:c.503T>A	ENSP00000507670.1:p.Ile168Asn
ENST00000683258.1:c.*224T>A	ENSP00000507448.1:n.*224T>A
ENST00000683339.1:c.401T>A	ENSP00000507758.1:p.Ile134Asn
ENST00000683403.1:c.503T>A	ENSP00000507896.1:p.Ile168Asn
ENST00000683429.1:c.110T>A	ENSP00000507697.1:p.Ile37Asn
ENST00000683665.1:c.503T>A	ENSP00000507068.1:p.Ile168Asn
ENST00000683789.1:c.503T>A	ENSP00000507012.1:p.Ile168Asn
ENST00000683882.1:c.503T>A	ENSP00000506735.1:p.Ile168Asn
ENST00000684024.1:c.*174T>A	ENSP00000507175.1:n.*174T>A
ENST00000684254.1:c.*229T>A	ENSP00000508001.1:n.*229T>A
ENST00000340941.11:c.503T>A MANE Select	ENSP00000343657.6:p.Ile168Asn
ENST00000340941.10:c.503T>A	ENSP00000343657.6:p.Ile168Asn
ENST00000505787.7:n.317T>A
ENST00000507169.5:n.429T>A
ENST00000509358.6:c.503T>A	ENSP00000420994.2:p.Ile168Asn
ENST00000510895.6:n.117T>A
ENST00000512218.6:c.503T>A	ENSP00000423202.2:p.Ile168Asn
ENST00000629193.2:c.503T>A	ENSP00000486535.1:p.Ile168Asn
NM_022132.4:c.503T>A	NP_071415.1:p.Ile168Asn
XM_005248567.1:c.503T>A	XP_005248624.1:p.Ile168Asn
XM_011543528.1:c.503T>A	XP_011541830.1:p.Ile168Asn
XM_011543529.1:c.503T>A	XP_011541831.1:p.Ile168Asn
NM_001363147.1:c.503T>A	NP_001350076.1:p.Ile168Asn
XM_011543529.2:c.503T>A	XP_011541831.1:p.Ile168Asn
XM_017009688.1:c.503T>A	XP_016865177.1:p.Ile168Asn
XR_001742172.1:n.543T>A
NM_022132.5:c.503T>A MANE Select	NP_071415.1:p.Ile168Asn