Canonical Allele Identifier: CA449814041

Gene: SKIC2

Linked Data

• MyVariant Identifiers: chr6:g.31937297C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969520C>T , CM000668.2:g.31969520C>T	GRCh38
NC_000006.11:g.31937297C>T , CM000668.1:g.31937297C>T	GRCh37
NC_000006.10:g.32045276C>T	NCBI36
NG_032652.1:g.15717C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2594C>T	ENSP00000419905.1:n.*2594C>T
ENST00000485349.6:n.4022C>T
ENST00000491994.2:c.*88C>T	ENSP00000417586.2:n.*88C>T
ENST00000494058.6:n.3848C>T
ENST00000697831.1:c.3477C>T	ENSP00000513453.1:p.Phe1159=
ENST00000697832.1:n.3699C>T
ENST00000697833.1:c.*494C>T	ENSP00000513454.1:n.*494C>T
ENST00000697834.1:n.4264C>T
ENST00000697835.1:c.*3064C>T	ENSP00000513455.1:n.*3064C>T
ENST00000697836.1:n.3900C>T
ENST00000697837.1:c.*662C>T	ENSP00000513456.1:n.*662C>T
ENST00000697838.1:c.3411C>T	ENSP00000513457.1:p.Phe1137=
ENST00000697839.1:n.4358C>T
ENST00000697840.1:c.3582C>T	ENSP00000513458.1:p.Phe1194=
ENST00000697841.1:n.4457C>T
ENST00000697842.1:n.3801C>T
ENST00000375394.7:c.3546C>T MANE Select	ENSP00000364543.2:p.Phe1182=
ENST00000375394.6:c.3546C>T	ENSP00000364543.2:p.Phe1182=
ENST00000465703.5:n.4276C>T
ENST00000470453.1:n.388C>T
ENST00000471818.1:n.475C>T
ENST00000474839.5:c.*2918C>T	ENSP00000420470.1:n.*2918C>T
ENST00000483553.5:c.1076C>T
ENST00000491994.1:c.635C>T
NM_006929.4:c.3546C>T	NP_008860.4:p.Phe1182=
XR_926301.3:n.3562C>T
NM_006929.5:c.3546C>T MANE Select	NP_008860.4:p.Phe1182=