Canonical Allele Identifier: CA363489780

Gene: SKIC2

Linked Data

• MyVariant Identifiers: chr6:g.31937109C>T (hg19) ; chr6:g.31969332C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969332C>T , CM000668.2:g.31969332C>T	GRCh38
NC_000006.11:g.31937109C>T , CM000668.1:g.31937109C>T	GRCh37
NC_000006.10:g.32045088C>T	NCBI36
NG_032652.1:g.15529C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2406C>T	ENSP00000419905.1:n.*2406C>T
ENST00000483553.6:c.*419C>T	ENSP00000420332.2:n.*419C>T
ENST00000485349.6:n.3928C>T
ENST00000491994.2:c.3452C>T	ENSP00000417586.2:p.Ala1151Val
ENST00000494058.6:n.3754C>T
ENST00000697831.1:c.3383C>T	ENSP00000513453.1:p.Ala1128Val
ENST00000697832.1:n.3605C>T
ENST00000697833.1:c.*400C>T	ENSP00000513454.1:n.*400C>T
ENST00000697834.1:n.4076C>T
ENST00000697835.1:c.*2970C>T	ENSP00000513455.1:n.*2970C>T
ENST00000697836.1:n.3783C>T
ENST00000697837.1:c.*568C>T	ENSP00000513456.1:n.*568C>T
ENST00000697838.1:c.3317C>T	ENSP00000513457.1:p.Ala1106Val
ENST00000697839.1:n.4170C>T
ENST00000697840.1:c.3488C>T	ENSP00000513458.1:p.Ala1163Val
ENST00000697841.1:n.4269C>T
ENST00000697842.1:n.3707C>T
ENST00000375394.7:c.3452C>T MANE Select	ENSP00000364543.2:p.Ala1151Val
ENST00000375394.6:c.3452C>T	ENSP00000364543.2:p.Ala1151Val
ENST00000465703.5:n.4088C>T
ENST00000470453.1:n.382+16C>T
ENST00000471818.1:n.381C>T
ENST00000474839.5:c.*2824C>T	ENSP00000420470.1:n.*2824C>T
ENST00000483553.5:c.888C>T
ENST00000485349.5:n.658C>T
ENST00000491994.1:c.447C>T
NM_006929.4:c.3452C>T	NP_008860.4:p.Ala1151Val
XR_001743586.2:n.3551C>T
XR_926301.3:n.3468C>T
NM_006929.5:c.3452C>T MANE Select	NP_008860.4:p.Ala1151Val