Canonical Allele Identifier: CA414941490
Gene: SRY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787370C>G , CM000686.2:g.2787370C>G GRCh38
NC_000024.9:g.2655411C>G , CM000686.1:g.2655411C>G GRCh37
NC_000024.8:g.2715411C>G NCBI36
NG_011751.1:g.5382G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12631C>G
ENST00000679825.1:n.482C>G
ENST00000680285.1:n.320-2379C>G
ENST00000680845.1:n.166-110C>G
ENST00000681787.1:n.106+12631C>G
ENST00000681940.1:n.106+12631C>G
ENST00000383070.2:c.234G>C MANE Select ENSP00000372547.1:p.Met78Ile
ENST00000383070.1:c.234G>C ENSP00000372547.1:p.Met78Ile
NM_003140.2:c.234G>C NP_003131.1:p.Met78Ile
NM_003140.3:c.234G>C MANE Select NP_003131.1:p.Met78Ile