Canonical Allele Identifier: CA446938274

Gene: SPINK5

Linked Data

• gnomAD v4: 5-148131288-A-T
• MyVariant Identifiers: chr5:g.147510851A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131288A>T , CM000667.2:g.148131288A>T	GRCh38
NC_000005.9:g.147510851A>T , CM000667.1:g.147510851A>T	GRCh37
NC_000005.8:g.147491044A>T	NCBI36
NG_009633.1:g.72317A>T , LRG_110:g.72317A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.2994A>T MANE Select	ENSP00000256084.7:p.Val998=
ENST00000256084.7:c.2994A>T	ENSP00000256084.7:p.Val998=
ENST00000359874.7:c.3084A>T	ENSP00000352936.3:p.Val1028=
NM_001127698.1:c.3084A>T	NP_001121170.1:p.Val1028=
NM_006846.3:c.2994A>T , LRG_110t1:c.2994A>T	NP_006837.2:p.Val998=
XM_011537550.1:c.3027A>T	XP_011535852.1:p.Val1009=
XM_011537551.1:c.3000A>T	XP_011535853.1:p.Val1000=
XM_011537551.2:c.3000A>T	XP_011535853.1:p.Val1000=
NM_001127698.2:c.3084A>T	NP_001121170.1:p.Val1028=
NM_006846.4:c.2994A>T MANE Select	NP_006837.2:p.Val998=