Canonical Allele Identifier: CA1619384406

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969590A= , CM000668.2:g.31969590A=	GRCh38
NC_000006.11:g.31937367A= , CM000668.1:g.31937367A=	GRCh37
NC_000006.10:g.32045346A=	NCBI36
NG_032652.1:g.15787A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2664A=	ENSP00000419905.1:n.*2664A=
ENST00000485349.6:n.4092A=
ENST00000491994.2:c.*158A=	ENSP00000417586.2:n.*158A=
ENST00000494058.6:n.3918A=
ENST00000697831.1:c.3547A=	ENSP00000513453.1:p.Met1183=
ENST00000697832.1:n.3769A=
ENST00000697833.1:c.*564A=	ENSP00000513454.1:n.*564A=
ENST00000697834.1:n.4334A=
ENST00000697835.1:c.*3134A=	ENSP00000513455.1:n.*3134A=
ENST00000697836.1:n.3970A=
ENST00000697837.1:c.*732A=	ENSP00000513456.1:n.*732A=
ENST00000697838.1:c.3481A=	ENSP00000513457.1:p.Met1161=
ENST00000697839.1:n.4428A=
ENST00000697840.1:c.3652A=	ENSP00000513458.1:p.Met1218=
ENST00000697841.1:n.4527A=
ENST00000697842.1:n.3871A=
ENST00000375394.7:c.3616A= MANE Select	ENSP00000364543.2:p.Met1206=
ENST00000375394.6:c.3616A=	ENSP00000364543.2:p.Met1206=
ENST00000465703.5:n.4346A=
ENST00000471818.1:n.545A=
ENST00000474839.5:c.*2988A=	ENSP00000420470.1:n.*2988A=
ENST00000483553.5:c.1146A=
ENST00000491994.1:c.705A=
NM_006929.4:c.3616A=	NP_008860.4:p.Met1206=
XR_926301.3:n.3632A=
NM_006929.5:c.3616A= MANE Select	NP_008860.4:p.Met1206=