Canonical Allele Identifier: CA364451986

Gene: EFHC1

Linked Data

• MyVariant Identifiers: chr6:g.52317501C>A (hg19) ; chr6:g.52452703C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52452703C>A , CM000668.2:g.52452703C>A	GRCh38
NC_000006.11:g.52317501C>A , CM000668.1:g.52317501C>A	GRCh37
NC_000006.10:g.52425460C>A	NCBI36
NG_016760.1:g.37508C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.589C>A MANE Select	ENSP00000360107.4:p.Gln197Lys
ENST00000480623.6:c.589C>A	ENSP00000434498.2:p.Gln197Lys
ENST00000635760.1:c.265C>A	ENSP00000489765.1:p.Gln89Lys
ENST00000635812.1:c.589C>A	ENSP00000490859.1:p.Gln197Lys
ENST00000635866.1:c.*458C>A	ENSP00000489866.1:n.*458C>A
ENST00000635911.1:n.850C>A
ENST00000635984.1:c.265C>A	ENSP00000489921.1:p.Gln89Lys
ENST00000635996.1:c.589C>A	ENSP00000490256.1:p.Gln197Lys
ENST00000636107.1:c.589C>A	ENSP00000489680.1:p.Gln197Lys
ENST00000636253.1:n.243C>A
ENST00000636311.1:n.483C>A
ENST00000636343.1:c.255C>A
ENST00000636379.1:c.301C>A	ENSP00000490622.1:p.Gln101Lys
ENST00000636398.1:c.256C>A	ENSP00000489654.1:p.Gln86Lys
ENST00000636489.1:c.532C>A	ENSP00000489998.1:p.Gln178Lys
ENST00000636702.1:c.559C>A	ENSP00000489623.1:p.Gln187Lys
ENST00000636954.1:c.532C>A	ENSP00000489966.1:p.Gln178Lys
ENST00000637089.1:c.589C>A	ENSP00000489854.1:p.Gln197Lys
ENST00000637200.1:c.*605C>A	ENSP00000490567.1:n.*605C>A
ENST00000637263.1:c.589C>A	ENSP00000489700.1:p.Gln197Lys
ENST00000637340.1:n.1257C>A
ENST00000637353.1:c.589C>A	ENSP00000490441.1:p.Gln197Lys
ENST00000637602.1:c.*290C>A	ENSP00000490074.1:n.*290C>A
ENST00000637849.1:n.653C>A
ENST00000637892.1:n.793C>A
ENST00000638075.1:c.-30C>A	ENSP00000490711.1:n.-30C>A
ENST00000371068.9:c.589C>A	ENSP00000360107.4:p.Gln197Lys
ENST00000480623.5:c.589C>A	ENSP00000434498.1:p.Gln197Lys
ENST00000538167.2:c.532C>A	ENSP00000444521.1:p.Gln178Lys
NM_001172420.1:c.532C>A	NP_001165891.1:p.Gln178Lys
NM_018100.3:c.589C>A	NP_060570.2:p.Gln197Lys
NR_033327.1:n.804C>A
NM_018100.4:c.589C>A MANE Select	NP_060570.2:p.Gln197Lys
NM_001172420.2:c.532C>A	NP_001165891.1:p.Gln178Lys
NR_033327.2:n.658C>A