Canonical Allele Identifier: CA2671129585
Gene: FRAS1 HGNC NCBI

Linked Data

gnomAD v4: 4-78264974-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78264974G>T , CM000666.2:g.78264974G>T GRCh38
NC_000004.11:g.79186128G>T , CM000666.1:g.79186128G>T GRCh37
NC_000004.10:g.79405152G>T NCBI36
NG_015812.1:g.212405G>T
NG_015812.2:g.212405G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325942.11:c.604-51G>T ENSP00000326330.6:n.604-51G>T
ENST00000502446.6:c.604-51G>T ENSP00000423645.2:n.604-51G>T
ENST00000508900.2:c.604-51G>T ENSP00000423809.2:n.604-51G>T
ENST00000682513.1:c.604-51G>T ENSP00000508201.1:n.604-51G>T
ENST00000683711.1:n.924-51G>T
ENST00000684159.1:c.604-51G>T ENSP00000506875.1:n.604-51G>T
ENST00000512123.4:c.604-51G>T MANE Select ENSP00000422834.2:n.604-51G>T
ENST00000264899.10:c.604-51G>T ENSP00000264899.7:n.604-51G>T
ENST00000325942.10:c.604-51G>T ENSP00000326330.6:n.604-51G>T
ENST00000502446.5:c.390-51G>T
ENST00000508900.1:c.131-51G>T
ENST00000512123.3:c.604-51G>T ENSP00000422834.2:n.604-51G>T
NM_001166133.1:c.604-51G>T NP_001159605.1:n.604-51G>T
NM_025074.6:c.604-51G>T NP_079350.5:n.604-51G>T
XM_006714314.1:c.604-51G>T XP_006714377.1:n.604-51G>T
XM_006714316.1:c.604-51G>T XP_006714379.1:n.604-51G>T
XM_006714316.3:c.604-51G>T XP_006714379.1:n.604-51G>T
NM_025074.7:c.604-51G>T MANE Select NP_079350.5:n.604-51G>T
NM_001166133.2:c.604-51G>T NP_001159605.1:n.604-51G>T