Canonical Allele Identifier: CA6737976

Gene: SCYL2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.100283076C>T , CM000674.2:g.100283076C>T	GRCh38
NC_000012.11:g.100676854C>T , CM000674.1:g.100676854C>T	GRCh37
NC_000012.10:g.99200985C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_017988.6:c.106C>T MANE Select	NP_060458.3:p.Arg36Ter
ENST00000360820.7:c.106C>T MANE Select	ENSP00000354061.2:p.Arg36Ter
NM_001317784.1:c.106C>T	NP_001304713.1:p.Arg36Ter
NM_001317784.2:c.106C>T	NP_001304713.1:p.Arg36Ter
NM_001330253.1:c.106C>T	NP_001317182.1:p.Arg36Ter
NM_001330253.2:c.106C>T	NP_001317182.1:p.Arg36Ter
NM_001330254.1:c.106C>T	NP_001317183.1:p.Arg36Ter
NM_001330254.2:c.106C>T	NP_001317183.1:p.Arg36Ter
NM_001330256.1:c.-550C>T	NP_001317185.1:n.-550C>T
NM_001330256.2:c.-550C>T	NP_001317185.1:n.-550C>T
NM_017988.4:c.106C>T	NP_060458.3:p.Arg36Ter
NM_017988.5:c.106C>T	NP_060458.3:p.Arg36Ter
ENST00000360820.6:c.106C>T	ENSP00000354061.2:p.Arg36Ter
ENST00000548392.5:c.-342-8427C>T	ENSP00000450294.1:n.-342-8427C>T
ENST00000549687.5:c.106C>T	ENSP00000448366.1:p.Arg36Ter
ENST00000550067.1:n.282C>T
ENST00000635101.1:c.106C>T	ENSP00000489123.1:p.Arg36Ter
XM_005269018.2:c.106C>T	XP_005269075.1:p.Arg36Ter
XM_011538559.1:c.-550C>T	XP_011536861.1:n.-550C>T
XM_011538560.1:c.106C>T	XP_011536862.1:p.Arg36Ter