Canonical Allele Identifier: CA455936826

Gene: KCTD7

Linked Data

• MyVariant Identifiers: chr7:g.66098267T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66633280T>C , CM000669.2:g.66633280T>C	GRCh38
NC_000007.13:g.66098267T>C , CM000669.1:g.66098267T>C	GRCh37
NC_000007.12:g.65735702T>C	NCBI36
NG_028110.1:g.9400T>C
NG_028110.2:g.9400T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.150T>C	ENSP00000275532.4:p.Pro50=
ENST00000449064.6:c.128T>C
ENST00000503687.2:c.144+4072T>C	ENSP00000421074.1:n.144+4072T>C
ENST00000638524.1:c.139+4072T>C
ENST00000638540.1:c.118+4072T>C
ENST00000639828.2:c.150T>C MANE Select	ENSP00000492240.1:p.Pro50=
ENST00000639879.1:c.150T>C	ENSP00000492161.1:p.Pro50=
ENST00000640234.1:c.20T>C
ENST00000640385.1:c.150T>C	ENSP00000491193.1:p.Pro50=
ENST00000640851.1:c.150T>C	ENSP00000492577.1:p.Pro50=
ENST00000275532.7:c.150T>C	ENSP00000275532.3:p.Pro50=
ENST00000443322.1:c.150T>C	ENSP00000411624.1:p.Pro50=
ENST00000449064.5:c.144+4072T>C	ENSP00000388463.1:n.144+4072T>C
ENST00000503687.1:c.144+4072T>C	ENSP00000421074.1:n.144+4072T>C
NM_001167961.2:c.150T>C	NP_001161433.1:p.Pro50=
NM_153033.4:c.150T>C	NP_694578.1:p.Pro50=
NM_153033.5:c.150T>C MANE Select	NP_694578.1:p.Pro50=